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Disease Ontology Browser
Fuchs' endothelial dystrophy (DOID:11555)
Alliance: disease page
Synonyms: FCED; Fuchs' corneal dystrophy; Fuchs' endothelial corneal dystrophy
Alt IDs: OMIM:136800, OMIM:610158, OMIM:613267, OMIM:613268, OMIM:613269, OMIM:613270, OMIM:613271, OMIM:615523, EFO:0003946, ICD10CM:H18.51, MESH:D005642, NCI:C84721, ORDO:98974, UMLS_CUI:C0016781
Definition: A corneal dystrophy characterized by accumulation of focal outgrowths (guttae) and thickening of Descemet's membrane, leading to corneal edema and loss of vision.

Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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MGI 6.17
The Jackson Laboratory