ocular albinism https://github.com/monarch-initiative/mondo/issues/6745 https://github.com/monarch-initiative/mondo/issues/7900 https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/albinism_ocular_type_i ICD9:270.2 ocular albinism (disease) GARD:0021124 NORD:1516 Albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. The classic type is X-linked (Nettleship-Falls), but an autosomal recessive form also exists. Ocular abnormalities may include reduced pigmentation of the iris, nystagmus, photophobia, strabismus, and decreased visual acuity. ocular albinism (disease) MONDO:0017304 MESH:D016117 DOID:0050633 MEDGEN:38147 UMLS:C0078917 HP:0001107 ICD10CM:E70.31 ocular albinism MedDRA:10065276 icd11.foundation:1147926040 Orphanet:284804 XLOA SCTID:26399002 disorder of melanin metabolism disorder of visual system