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Summary Literature (2)
DOID:11555 - Fuchs' endothelial dystrophy


Disease Ontology 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.

Synonyms: FCED, Fuchs' corneal dystrophy, Fuchs' endothelial corneal dystrophy

In OMIM:
OMIM:136800 - CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1; FECD1
OMIM:610158 - CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2; FECD2
OMIM:613267 - CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3; FECD3
OMIM:613268 - CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4; FECD4
OMIM:613269 - CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 5; FECD5
OMIM:613270 - CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6; FECD6
OMIM:613271 - CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 7; FECD7
OMIM:615523 - CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 8; FECD8

In Mondo Disease Ontology:
MONDO:0005321 - Fuchs' endothelial dystrophy

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : slc4a11, zeb1, agbl1, col8a2, tcf4

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): corneal endothelial dystrophy (is_a)