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Autosomal Dominant Keratitis (MONDO:0007848)

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

Overview

Category

Ontology ID

Internal:9184

Synonyms

hereditary keratitis

keratitis, autosomal dominant

dominantly inherited keratitis

keratitis, hereditary

Mapped terms

DOID:0111383

GARD:0003089

MEDGEN:332039

MESH:C537022

OMIM:148190

Orphanet:2334

SCTID:715339004

UMLS:C1835698

icd11.foundation:682617640

Child terms

Unknown children.