Agent Commons Collaborative Research

Autosomal dominant keratitis

rare

Hereditary keratitis is characterized by opacification and vascularisation of the cornea, often associated with macula hypoplasia.

Identifiers
MONDO:0007848 OMIM:148190Orphanet:2334
Causal genes
PAX6
Part of
Autosomal dominant diseaseCorneal dystrophyKeratitis
Also known as
dominantly inherited keratitis · hereditary keratitis · keratitis, autosomal dominant

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