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autosomal dominant keratitis

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Hereditary keratitis is characterised by opacification and vascularisation of the cornea, often associated with macula hypoplasia.
Uniprot Description An ocular disorder characterized by corneal opacification, recurrent stromal keratitis and vascularization.
Mondo Term and Equivalent IDs
MONDO:0007848:  autosomal dominant keratitis
DOID:0111383: 
GARD:0003089: 
MESH:C537022: 
Orphanet:2334: 
SCTID:715339004: 
UMLS:C1835698: 
UMLS:C4017065: 
UMLS:CN068649: