X-linked endothelial corneal dystrophy Disease Ontology Browser

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Disease Ontology Browser

X-linked endothelial corneal dystrophy (DOID:0060446)
Alliance: disease page
Synonyms: XECD
Alt IDs: OMIM:300779, ICD10CM:H18.5, MESH:C567587, ORDO:293621
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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