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 Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) 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)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease 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 Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes 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 Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:bone development disease
go back to main search page
Accession:EFO:0005541 term browser browse the term
Definition:A bone disease that results_in abnormal growth and development located_in bone or located_in cartilage. A disease involving the bone development.
Synonyms:exact_synonym: DOID:0080006;   bone development disease or disorder;   disease of bone development;   disease or disorder of bone development;   disorder of bone development;   http://identifiers.org/medgen/2309;   http://identifiers.org/snomedct/371521007;   http://linkedlifedata.com/resource/umls/id/C0005941
 xref: DOID:0080006;   ICD10:Q68;   MEDGEN:2309;   MONDO:0005497;   SCTID:371521007;   UMLS:C0005941


show annotations for term's descendants           Sort by:
Term paths to the root
Path 1
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          disorder of development or morphogenesis 0
            bone development disease 0
              angioosteohypotrophic syndrome 0
              brachydactyly-elbow wrist dysplasia syndrome 0
              developmental dysplasia of the hip 0
              dysostosis + 0
              microcephalic osteodysplastic dysplasia, Saul-Wilson type 0
              osteochondrodysplasia + 0
              spondylocarpotarsal synostosis syndrome 0
Path 2
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          musculoskeletal system disease 0
            skeletal system disease 0
              bone disease 0
                bone development disease 0
                  angioosteohypotrophic syndrome 0
                  brachydactyly-elbow wrist dysplasia syndrome 0
                  developmental dysplasia of the hip 0
                  dysostosis + 0
                  microcephalic osteodysplastic dysplasia, Saul-Wilson type 0
                  osteochondrodysplasia + 0
                  spondylocarpotarsal synostosis syndrome 0
paths to the root