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:Fuchs' endothelial dystrophy
go back to main search page
Accession:EFO:MONDO:0005321 term browser browse the term
Definition:Fuchs endothelial corneal dystrophy (FECD) is the most frequent form of posterior corneal dystrophy and is characterized by excrescences on a thickened Descemet membrane (corneal guttae), generalized corneal edema, with gradually decreased visual acuity.
Synonyms:exact_synonym: DOID:11555;   Endoepithelial corneal dystrophy;   FCED;   FECD;   Fuchs' corneal dystrophy;   NCIT:C84721;   Orphanet:98974;   http://identifiers.org/medgen/4800;   http://identifiers.org/mesh/D005642;   http://identifiers.org/snomedct/193839007;   http://linkedlifedata.com/resource/umls/id/C0016781;   https://omim.org/phenotypicSeries/PS136800;   late hereditary endothelial dystrophy
 related_synonym: Fuchs endothelial corneal dystrophy
 alt_id: MONDO:0005321
 xref: DOID:11555;   GARD:10018;   MEDGEN:4800;   MESH:D005642;   MIM:PS136800;   NCI:C84721;   ORDO:98974;   SCTID:193839007;   UMLS:C0016781


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
          genetic disorder 0
            Fuchs' endothelial dystrophy 0
              corneal dystrophy, Fuchs endothelial, 3 0
              corneal dystrophy, Fuchs endothelial, 4 0
Path 2
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          head and neck disorder 0
            disease of orbital region 0
              eye disease 0
                corneal disease 0
                  corneal dystrophy 0
                    posterior corneal dystrophy 0
                      Fuchs' endothelial dystrophy 0
                        corneal dystrophy, Fuchs endothelial, 3 0
                        corneal dystrophy, Fuchs endothelial, 4 0
paths to the root