Fuchs' endothelial dystrophy

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Echinobase

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

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

MIM:

MIM:136800 - corneal dystrophy, fuchs endothelial, 1; fecd1
MIM:615523 - corneal dystrophy, fuchs endothelial, 8; fecd8

MIM:136800 - corneal dystrophy, fuchs endothelial, 1; fecd1

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)