X-linked endothelial corneal dystrophy

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Summary

Literature (0)

DOID:0060446 - X-linked endothelial corneal dystrophy

Disease Ontology Definition:A corneal endothelial dystrophy that is characterized by congenital ground glass corneal clouding or a diffuse corneal haze, and blurred vision in male patients.

Synonyms: XECD,

Xenbase 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

:

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010426 - X-linked endothelial corneal dystrophy

MONDO:0010426 - X-linked endothelial corneal dystrophy

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): corneal endothelial dystrophy (is_a)