oculocutaneous albinism type 2 https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/4038/oculocutaneous-albinism-type-2 https://www.malacards.org/card/albinism_oculocutaneous_type_ii oculocutaneous albinism, tyrosinase-positive MONDO:0008746 Albinoidism DOID:0070096 MESH:C537730 albinism, oculocutaneous, type 2 oculocutaneous albinism type 2 Orphanet:79432 MEDGEN:82810 albinism, oculocutaneous, type II albinism, oculocutaneous, type II, modifier of GARD:0004038 oculocutaneous albinism tyrosinase positive icd11.foundation:2019316252 Oculocutaneous albinism type 2 (OCA2) is a type of OCA and the most common form of OCA seen in the African population, characterized by variable hypopigmentation of the skin and hair, numerous characteristic ocular changes and misrouting of the optic nerves at the chiasm. OCA2 OMIM:203200 tyrosinase-positive oculocutaneous albinism UMLS:C0268495 oculocutaneous albinism