Disease Summary help help Associated Targets (1)Tbio1 Explore Associated Targets list GARD Rare open_in_new 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: open_in_newGARD:0003089: open_in_newMESH:C537022: open_in_newOMIM:148190: KERATITIS, HEREDITARYopen_in_newOrphanet:2334: SCTID:715339004: open_in_newUMLS:C1835698: open_in_newUMLS:C4017065: open_in_newUMLS:CN068649: open_in_new