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

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

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0005321 - mesonephric smooth muscle tissue

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