Send us a Message



 Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap)  (beta) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer) Overgo Probe Designer
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease COVID-19 Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models PhenoMiner (Quantitative Phenotypes) Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes GERRC (Gene Editing Rat Resource Center) Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Poster Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

GENE - TERM ANNOTATION REPORT

2001 Annotations Found.

An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151851248 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12740078 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:21034864 PMID:25525159 PMID:25741868 PMID:26799313 PMID:27398169 PMID:28492532 PMID:30884209


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21403699 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9684421 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:15967699 PMID:16199547 PMID:16283883 PMID:18414213 PMID:22677543 PMID:23551039 PMID:25741868 PMID:28492532 PMID:30120852 PMID:33640437


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151769537 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151819098 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16283883 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151759590 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151720036 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16283883 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782603 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22484412 PMID:22745856 PMID:25741868 PMID:25982861 PMID:27022412 PMID:28492532 PMID:34470610


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Levy E, etal., Life Sci. 2007 Mar 27;80(16):1472-83. Epub 2007 Jan 20.
  • The annotation has been inferred from sequence orthology with Atp7b (Rattus norvegicus) [(IAGP) inferred by association of genotype and phenotype]
  • 24 additional annotations were made from Levy E, etal., Life Sci. 2007 Mar 27;80(16):1472-83. Epub 2007 Jan 20.
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: DNA:deletion:exon


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Sasaki N, etal., Biochem Biophys Res Commun 1994 Jul 15;202(1):512-8.
  • The annotation has been inferred from sequence orthology with Atp7b (Rattus norvegicus) [(IDA) inferred from direct assay]
  • 2 additional annotations were made from Sasaki N, etal., Biochem Biophys Res Commun 1994 Jul 15;202(1):512-8.
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:10686180 PMID:10790207 PMID:10830865 PMID:10982773 PMID:11157799 PMID:11405812 PMID:11472373 PMID:11803042 PMID:11854914 PMID:11985593 PMID:12228238 PMID:12544487 PMID:12820478 PMID:14574444 PMID:14579150 PMID:14998371 PMID:15135151 PMID:15147237 PMID:15911138 PMID:16133174 PMID:16607473 PMID:16824500 PMID:16932613 PMID:17182432 PMID:17276780 PMID:17634212 PMID:17919502 PMID:18371106 PMID:18779302 PMID:19888908 PMID:20647314 PMID:21146535 PMID:21242307 PMID:21364284 PMID:21406592 PMID:22130675 PMID:22455587 PMID:22565294 PMID:22677543 PMID:22802922 PMID:22945834 PMID:22981378 PMID:23235335 PMID:23333878 PMID:23789284 PMID:23843956 PMID:23963605 PMID:24094725 PMID:24892424 PMID:25003971 PMID:25134866


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21404038 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14689409 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151807064 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151884143 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16283883 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151822354 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126915632 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126911180 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126909926 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126911137 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126913824 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151756744 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23843956 PMID:27398169 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13213038 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151886266 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:15024742 PMID:21796144 PMID:28492532 PMID:30120852 PMID:9671269


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15121920 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15109474 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151779778 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16283883 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151844171 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:11093740 PMID:15952988 PMID:23843956 PMID:27398169 PMID:28492532 PMID:30702195


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127322068 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28888375 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127292756 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127320073 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127290208 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127321353 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127292768 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151803612 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15198893 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15123746 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127292779 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15111008 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14738449 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569234 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:11405812 PMID:18414213 PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127314553 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13520153 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30556376


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127287332 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127291285 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127305545 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151846048 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9684438 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:18414213 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127288367 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151773203 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:17576681 PMID:27022412 PMID:28492532 PMID:9536098


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15187716 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127305502 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127305409 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151880563 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16283883 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13437178 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15171547 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38476339 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127288156 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10041368 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:10447265 PMID:10502777 PMID:10994503 PMID:11093740 PMID:11690702 PMID:11857545 PMID:12557139 PMID:12955875 PMID:15024742 PMID:15952988 PMID:15967699 PMID:16207219 PMID:16283883 PMID:16791614 PMID:17897870 PMID:18855987 PMID:20082719 PMID:23518715 PMID:23789284 PMID:23982005 PMID:25497208 PMID:25741868 PMID:27941192 PMID:28492532 PMID:31708252 PMID:32043565 PMID:32067425 PMID:7626145 PMID:8298640 PMID:8298641 PMID:8533760 PMID:8938442 PMID:9311736 PMID:9887381


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150536731 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127316863 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127325691 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15152816 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151870181 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150536719 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127301438 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15126530 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127297406 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127321474 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127299779 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127289160 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15158150 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15118989 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9684425 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:18414213 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127303670 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127309981 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26888452 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21075292 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16644258 PMID:24253677 PMID:25741868 PMID:28492532 PMID:29063292


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9589246 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10406672 PMID:10544227 PMID:11690702 PMID:11857545 PMID:12557139 PMID:15967699 PMID:16133174 PMID:16233999 PMID:16791614 PMID:16796414 PMID:17433323 PMID:17717039 PMID:17919502 PMID:18414213 PMID:19596473 PMID:22240481 PMID:22692182 PMID:23333878 PMID:24253677 PMID:25741868 PMID:27398169 PMID:28492532 PMID:8936442 PMID:8938442 PMID:9311736 PMID:9887381


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295380 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11551849 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127302499 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127290721 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127291458 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15125172 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15097951 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12836344 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906278 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156239460 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127270248 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127311835 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127300443 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15101805 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15171329 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150536730 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127301738 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127321113 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127303817 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127318991 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38489414 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127308795 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295517 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295474 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15186654 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127307046 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127275277 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906612 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906602 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:41407453 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:10502777 PMID:16283883 PMID:23518715 PMID:25327413 PMID:28492532 PMID:29418065


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21072547 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15181237 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620695 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15104030 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127296614 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15141215 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127267739 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569237 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10502777 PMID:11857545 PMID:15967699 PMID:17272994 PMID:18483695 PMID:20517649 PMID:21610751 PMID:21682854 PMID:22692182 PMID:22774841 PMID:23518715 PMID:23551039 PMID:23774950 PMID:25741868 PMID:27022412 PMID:28488633 PMID:28492532 PMID:28753182 PMID:29163329 PMID:30230192 PMID:31059521 PMID:8938442 PMID:9671269 PMID:9837819


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13790804 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:24517292 PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127308324 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295985 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623115 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15141459 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15108886 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127292759 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151783690 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23430908 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328056 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15200157 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127289319 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15198048 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127307161 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15139563 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15125357 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127326128 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13488909 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8557729 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:15557537 PMID:21956287 PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38496364 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14719608 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38462309 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127277630 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156241199 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127267695 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13521578 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15138963 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12740581 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:11690702 PMID:12557139 PMID:15967699 PMID:16283883 PMID:28492532 PMID:9311736


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11616846 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38476321 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127324746 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127335382 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15131162 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888098 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127298651 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26892188 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532 PMID:29321352


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12740251 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:15524314 PMID:27022412


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14689407 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15142073 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26918102 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14738889 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13538666 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15140081 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13613558 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10052418 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23518715 PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14690265 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15132465 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785084 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23518715 PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15143432 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127313302 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13519451 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12740446 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15132394 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13627200 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328307 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127267762 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906277 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38499639 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21075297 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15117135 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151833141 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15145924 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12906430 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23518715 PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328309 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328312 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23389864 PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15154135 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15189066 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15188843 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15147846 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127332807 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888811 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151769753 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12898792 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127267751 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16283883 PMID:28492532 PMID:29321352


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127310227 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14689423 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127333079 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15150716 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15187507 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13792195 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22692182 PMID:23518715 PMID:24253677 PMID:25741868 PMID:28492532 PMID:9671269


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15178110 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625240 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11551641 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10403417 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906611 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127320095 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15145796 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328313 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328328 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784541 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532 PMID:8938442


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328326 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22677543 PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred from direct assay (IDA)
    		•  
  • The annotation was made from Meng Y, etal., Biochim Biophys Acta 2004 Nov 5;1690(3):208-19.
  • 14 additional annotations were made from Meng Y, etal., Biochim Biophys Acta 2004 Nov 5;1690(3):208-19.
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Qualifier: treatment


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred from direct assay (IDA)
    		•  
  • The annotation was made from Merle U, etal., Scand J Gastroenterol. 2006 Aug;41(8):974-82. doi: 10.1080/00365520600554790.
  • 2 additional annotations were made from Merle U, etal., Scand J Gastroenterol. 2006 Aug;41(8):974-82. doi: 10.1080/00365520600554790.
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Qualifier: treatment


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127298178 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13613552 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127300044 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15128067 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328308 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15137041 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328329 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22677543 PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11636781 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:18373411 PMID:20465995 PMID:22692182 PMID:23235335 PMID:24253677 PMID:25741868 PMID:27935710 PMID:28492532 PMID:30097039 PMID:31059521 PMID:31449670 PMID:31751128


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127322678 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127310100 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127334343 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127287595 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13519514 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906280 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328317 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:17949296 PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328321 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:27398169


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328331 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127298771 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15148407 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11658389 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15130936 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15114333 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127337841 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38598419 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22484412 PMID:22692182 PMID:23518715 PMID:28492532 PMID:9222767


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328323 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127320319 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13621438 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652930 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26891353 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532 PMID:30655162


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127313735 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127288049 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127231047 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127233994 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785270 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10502776 PMID:14616767 PMID:26752957 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127294037 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127275562 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151808198 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25497208 PMID:28492532 PMID:29085216


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127312125 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127338231 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623666 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127291879 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906607 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151861992 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10041629 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson's disease
  • Original References(s): PMID:14962673 PMID:17949296


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569242 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13528279 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151777341 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615232 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15160837 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127293428 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127337251 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126734592 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13477611 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569230 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:18373411 PMID:20465995 PMID:21794208 PMID:23235335 PMID:23518715 PMID:24253677 PMID:25637381 PMID:25741868 PMID:28492532 PMID:30097039 PMID:31169307 PMID:32248359


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127291629 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328324 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:18034201 PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26893100 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151881651 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155944809 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906603 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127293595 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15138878 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127318040 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151718711 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16283883 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127292771 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127320634 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569261 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23518715 PMID:28492532 PMID:28776642


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26922773 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127266053 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26890845 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15101806 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127233350 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127300355 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127286559 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295278 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127318221 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647869 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127237836 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786983 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:12325021 PMID:22677543 PMID:22687675 PMID:23567103 PMID:28492532 PMID:32043565


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788600 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10544227 PMID:22692182 PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151880756 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783462 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:21034864 PMID:25089800 PMID:25741868 PMID:27398169 PMID:27706781 PMID:28492532 PMID:29321352 PMID:30702195


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906270 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127235054 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569231 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson's disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10041367 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:19371217 PMID:22677543 PMID:23518715 PMID:24094725 PMID:25741868 PMID:28492532 PMID:9311736


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127275540 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127288729 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12849713 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:15523622 PMID:17949296 PMID:22692182 PMID:23235335 PMID:24253677 PMID:25741868 PMID:27022412 PMID:28492532 PMID:34470610 PMID:8533760


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156393205 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12740579 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11599536 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151724951 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156219359 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127301369 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295913 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127296208 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11662228 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12740054 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:11216666 PMID:16199547 PMID:16283883 PMID:18371106 PMID:18483695 PMID:21645214 PMID:21682854 PMID:23518715 PMID:25741868 PMID:28492532 PMID:32532207 PMID:8533760 PMID:9311736 PMID:9801873


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Schmitt F, etal., PLoS One. 2013 Dec 17;8(12):e82323. doi: 10.1371/journal.pone.0082323. eCollection 2013.
  • The annotation has been inferred from sequence orthology with Atp7b (Rattus norvegicus) [(IAGP) inferred by association of genotype and phenotype]
  • 4 additional annotations were made from Schmitt F, etal., PLoS One. 2013 Dec 17;8(12):e82323. doi: 10.1371/journal.pone.0082323. eCollection 2013.
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: compared to LEA/Hok


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612798 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623878 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127277504 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12739582 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:21454443


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619437 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11551400 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151724995 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11661388 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12740558 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127292763 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Wu J, etal., Nat Genet 1994 Aug;7(4):541-5.
  • The annotation has been inferred from sequence orthology with Atp7b (Rattus norvegicus) [(IAGP) inferred by association of genotype and phenotype]
  • 4 additional annotations were made from Wu J, etal., Nat Genet 1994 Aug;7(4):541-5.
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Okayasu T, etal., Pediatr Res. 1992 Mar;31(3):253-7. doi: 10.1203/00006450-199203000-00011.
  • The annotation has been inferred from sequence orthology with Atp7b (Rattus norvegicus) [(IAGP) inferred by association of genotype and phenotype]
  • 10 additional annotations were made from Okayasu T, etal., Pediatr Res. 1992 Mar;31(3):253-7. doi: 10.1203/00006450-199203000-00011.
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11621141 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Fujiyoshi J, etal., Sci Rep. 2019 Feb 7;9(1):1535. doi: 10.1038/s41598-018-38275-y.
  • The annotation has been inferred from sequence orthology with Atp7b (Rattus norvegicus) [(IAGP) inferred by association of genotype and phenotype]
  • 31 additional annotations were made from Fujiyoshi J, etal., Sci Rep. 2019 Feb 7;9(1):1535. doi: 10.1038/s41598-018-38275-y.
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: compared to LEA/Hok


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15192711 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9681935 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623705 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127333885 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12739313 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16283883 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26923278 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569227 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson's disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127232963 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12740609 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13613545 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622464 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650049 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12898468 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127329967 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:41405849 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12844894 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649703 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127254942 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619608 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156066540 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127288209 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618596 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38482986 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127288699 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127273697 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127268661 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:18034201 PMID:18760268 PMID:19700008 PMID:22692182 PMID:23843956 PMID:25741868 PMID:27022412 PMID:27398169 PMID:28492532 PMID:30384382 PMID:9452121


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650917 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618934 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11661701 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12740197 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127329654 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615567 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623215 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11616960 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127315555 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619337 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13527086 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618198 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11659038 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127278988 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906269 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127232739 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612973 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13472740 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625301 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11659318 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11661402 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151782143 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38496204 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10041577 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson's disease
  • Original References(s): PMID:23518715 PMID:8298641


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625890 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9684413 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:18414213 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625276 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127263064 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12739271 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127292775 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16088907 PMID:23518715 PMID:25741868 PMID:26275891 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13520336 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11654477 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625747 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11664297 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127312535 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151871319 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625466 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156313312 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:15523622 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11663549 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649904 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256851 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11658329 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127326517 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11602067 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13494958 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127235071 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12893430 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:15967699 PMID:16283883 PMID:18371106 PMID:23486543 PMID:25741868 PMID:26752957 PMID:28492532 PMID:29649982 PMID:30723317


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328301 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328303 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22484412 PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619360 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:15024742 PMID:15952988 PMID:17576681 PMID:19118915 PMID:19371217 PMID:20967755 PMID:22677543 PMID:23518715 PMID:23962630 PMID:23982005 PMID:24661374 PMID:25497208 PMID:25741868 PMID:28443131 PMID:28492532 PMID:31059521 PMID:9536098


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328295 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22677543 PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328296 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22677543 PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328297 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22677543 PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127242752 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127242518 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26905824 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127232869 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127329125 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9684424 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10544227 PMID:15967699 PMID:18403153 PMID:18414213 PMID:20517649 PMID:21682854 PMID:22677543 PMID:22940187 PMID:23518715 PMID:25741868 PMID:26782526 PMID:26819605 PMID:27982432 PMID:27992490 PMID:28492532 PMID:9199563


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127300700 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256033 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38465873 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256908 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12740431 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:14966923 PMID:18203200 PMID:20082719 PMID:22692182 PMID:24253677 PMID:25741868 PMID:26483271 PMID:27022412 PMID:28212618 PMID:28492532 PMID:30702195 PMID:8938442


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127280300 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127254615 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127280087 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127230762 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127232223 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127273489 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127232395 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127244369 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26916670 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127336706 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8557717 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10502777 PMID:11243728 PMID:18414213 PMID:21610751 PMID:22240481 PMID:22692182 PMID:23518715 PMID:24253677 PMID:25741868 PMID:26207595 PMID:28492532 PMID:7626145


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8557724 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10942420 PMID:11243728 PMID:14761325 PMID:15952988 PMID:16088907 PMID:16603785 PMID:16868807 PMID:17587212 PMID:18728530 PMID:21645214 PMID:22692182 PMID:23333878 PMID:24253677 PMID:25741868 PMID:27022412 PMID:27930511 PMID:28212618 PMID:28492532 PMID:30232804 PMID:7626145 PMID:8533760 PMID:9837819


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11543809 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:17823867 PMID:23551039 PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8639316 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127260895 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127326954 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12740124 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16199547 PMID:16283883 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328305 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:18203200 PMID:22692182 PMID:24253677 PMID:25741868 PMID:9671269


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127247240 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10041602 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:11874474 PMID:15024742 PMID:16283883 PMID:17272994 PMID:17587212 PMID:18034201 PMID:18483695 PMID:20485189 PMID:21610751 PMID:21682854 PMID:22240481 PMID:22692182 PMID:23518715 PMID:23551039 PMID:25741868 PMID:28492532 PMID:8931691


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127281510 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10041579 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:10544227 PMID:16283883 PMID:17317524 PMID:17949296 PMID:23518715 PMID:25741868 PMID:27398169 PMID:28492532 PMID:7626145


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13518099 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:17576681 PMID:21707886 PMID:22019423 PMID:22677543 PMID:28492532 PMID:9536098


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127263362 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127232318 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127274878 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10041404 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10502776 PMID:10544227 PMID:12885331 PMID:17264425 PMID:21610751 PMID:22484412 PMID:22692182 PMID:23333878 PMID:23518715 PMID:24094725 PMID:25741868 PMID:25982861 PMID:26799313 PMID:28492532 PMID:31059521


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10041486 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16133174 PMID:16283883 PMID:17264425 PMID:21034864 PMID:21645214 PMID:23518715 PMID:23551039 PMID:24094725 PMID:25525159 PMID:25741868 PMID:28492532 PMID:30426382 PMID:31059521 PMID:9887381


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569226 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569228 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:11175281 PMID:11405812 PMID:18414213 PMID:25741868 PMID:28492532 PMID:7626145 PMID:9311736


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569229 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8557732 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:11093740 PMID:15024742 PMID:17634212 PMID:17897870 PMID:18414213 PMID:21832955 PMID:22692182 PMID:23982005 PMID:25741868 PMID:28492532 PMID:9311736


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784964 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10502777 PMID:22692182 PMID:23235335 PMID:23518715 PMID:24253677 PMID:25741868 PMID:28492532 PMID:31059521


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127328789 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127260355 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569241 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:11175281 PMID:18414213 PMID:25741868 PMID:28492532 PMID:7626145 PMID:8533760 PMID:9887381


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127261511 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13521723 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569235 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532 PMID:7626145


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569240 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10502777 PMID:15952988 PMID:16088907 PMID:17300695 PMID:17823867 PMID:18414213 PMID:25741868 PMID:28492532 PMID:7626145 PMID:8533760 PMID:8938442 PMID:9311736 PMID:9801873


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8557728 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10544227 PMID:15523622 PMID:16791614 PMID:17325640 PMID:20517649 PMID:22240481 PMID:22308153 PMID:22692182 PMID:25741868 PMID:26819605 PMID:28492532 PMID:8533760 PMID:9801873


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127262858 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127250156 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127274529 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127282206 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127246448 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127264432 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569243 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16088907 PMID:18414213 PMID:25741868 PMID:28492532 PMID:8533760


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569254 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:14966923 PMID:18414213 PMID:25741868 PMID:28492532 PMID:7626145


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569238 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14711046 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16199547 PMID:16283883 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127250704 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38499542 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569249 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson's disease
  • Original References(s): PMID:16088907 PMID:23518715 PMID:24094725 PMID:25741868 PMID:28492532 PMID:7626145


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256515 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127253040 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127279052 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127243407 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16416207 PMID:17410460 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8557731 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:15523622 PMID:15845031 PMID:16283883 PMID:17410460 PMID:18371106 PMID:18403153 PMID:19172127 PMID:22677543 PMID:23518715 PMID:25525159 PMID:25741868 PMID:26580967 PMID:28492532 PMID:8938442 PMID:9801873


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127279139 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127253374 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16283883 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127247977 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569236 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16088907 PMID:18414213 PMID:25741868 PMID:28492532 PMID:7626145


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256952 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127283038 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Sánchez-Monteagudo A, etal., Clin Genet. 2020 Feb 11. doi: 10.1111/cge.13719.
  • 2 additional annotations were made from Sánchez-Monteagudo A, etal., Clin Genet. 2020 Feb 11. doi: 10.1111/cge.13719.
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: DNA:mutations:multiple:


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569247 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127276479 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11609769 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888810 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38497561 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127239249 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127259923 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10041417 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16567646 PMID:20333758 PMID:22046264 PMID:22692182 PMID:23551039 PMID:24094725 PMID:25741868 PMID:28492532 PMID:31059521 PMID:7626145


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127231217 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127258224 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127259018 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888739 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127232244 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888737 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38483171 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127273999 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127240007 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127283456 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888809 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38456173 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127238431 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888740 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127278697 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127252372 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127258419 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127280452 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127248884 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13521651 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:25741868


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38493626 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127279495 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888735 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127282404 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127258394 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:26031236 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127279485 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127278377 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127278694 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127250426 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127258876 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782464 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:17949296 PMID:20517649


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127274713 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888812 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127254076 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10441329 PMID:16283883 PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127245778 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127249247 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127251146 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127245790 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791614 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:11721763 PMID:18373411 PMID:20453399 PMID:21645214 PMID:21982967 PMID:25046119


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782876 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22484412


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888738 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791687 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16696937 PMID:21645214


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13789013 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40889329 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127251950 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791177 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23518715


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783198 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127279501 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784563 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784329 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16423615


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791052 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23789284


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785160 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23518715


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788304 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787618 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:18373411 PMID:25525159


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791034 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23843956


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782701 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10942420 PMID:26660341 PMID:7626145 PMID:9837819


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786175 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:20931554 PMID:27022412


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13789873 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:21796144 PMID:23843956 PMID:25376582 PMID:27398169


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13789177 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788823 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:27022412


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127231032 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13790299 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13789721 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22484412


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791366 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:26782526


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787945 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785414 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:15952988


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791565 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:11180609 PMID:11690702 PMID:12557139 PMID:20517649 PMID:22240481 PMID:22692182 PMID:24253677


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788965 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787113 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16684691


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784162 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22677543


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782718 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787031 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:22240481 PMID:9482578


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127232690 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127273579 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127272531 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127281460 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13828830 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127248664 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127246572 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127239527 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127258635 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783072 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:21454443


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783038 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784582 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786093 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791961 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:10790207 PMID:21454443


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782474 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791989 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785024 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127279553 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788697 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:23518715


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786144 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:24094725


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13790190 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:17587212 PMID:21645214 PMID:22692182 PMID:24253677


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791538 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16088907 PMID:23518715


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788587 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16088907


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782406 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13784457 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786671 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:20491539 PMID:25525159 PMID:26782526 PMID:27022412


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785493 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:27022412


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787468 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:27022412


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888742 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127244607 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127239586 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127283956 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127263349 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256063 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:28492532


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791085 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786608 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788554 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13789638 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:17949296 PMID:25678388


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13790296 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16088907 PMID:22692182


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13792243 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:18034201 PMID:27982432


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13791557 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13788234 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13785897 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:20517649 PMID:25525159


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13782827 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:15811015 PMID:22692182 PMID:24253677


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13786747 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:17587212 PMID:21645214 PMID:25525159


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13783005 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13792012 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:21219664 PMID:23551039


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13790732 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:16088907 PMID:21454443


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13789367 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used to annotate ATP7B
  • Curation Notes: ClinVar Annotator: match by term: Wilson disease
  • Original References(s): PMID:24094725


    • An association has been curated linking ATP7B and Wilson disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13787736 (Homo sapiens)
  • 49 RGD objects have been annotated to Wilson disease  (DOID:893)
  • 22 papers in RGD have been used