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