has material basis in germline mutation in TYRP1 oculocutaneous albinism type 3 https://www.malacards.org/card/albinism_oculocutaneous_type_iii MEDGEN:87450 OMIM:203290 Red oculocutaneous albinism rufous oculocutaneous albinism SCTID:63450009 icd11.foundation:1565320806 OMIM:278400 MESH:C537731 TYRP1 oculocutaneous albinism oculocutaneous albinism caused by mutation in TYRP1 ROCA GARD:0004039 Xanthism albinism, oculocutaneous, type III xanthous oculocutaneous albinism rufous OCA MONDO:0008747 Type 3 oculocutaneous albinism (OCA3) is a form of oculocutaneous albinism (OCA) characterized by rufous or brown albinism and occurring mainly in the African population. UMLS:C0342683 albinism, oculocutaneous, type 3 DOID:0070097 Orphanet:79433 OCA3 ICD9:270.2 oculocutaneous albinism type 3 oculocutaneous albinism