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Summary Literature (0)
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

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

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0005321 - Fuchs' endothelial dystrophy

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

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): corneal endothelial dystrophy (is_a)