has characteristic has characteristic X-linked recessive inheritance ocular albinism X-linked recessive disease X-linked recessive ocular albinism https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/6562 Nettleship-Falls type ocular albinism SCTID:78642008 X-linked recessive ocular albinism (XLOA) is a rare disorder characterized by ocular hypopigmentation, foveal hypoplasia, nystagmus, photodysphoria, and reduced visual acuity in males. MESH:C537863 MEDGEN:90991 OMIM:300500 UMLS:C0342684 MONDO:0021019 ocular albinism type 1 GARD:0008471 Orphanet:54 X-linked ocular albinism NCIT:C118785 albinism, ocular, type I ocular albinism, Nettleship-Falls type XLOA OA1 ICD9:270.2 albinism, ocular, type 1 ocular albinism, type I, Nettleship-Falls type icd11.foundation:846740259 Nettleship-Falls syndrome albinism GPR143-related foveal hypoplasia