oculocutaneous albinism type 5 https://www.malacards.org/card/albinism_oculocutaneous_type_v SCTID:722057000 Orphanet:370091 UMLS:C3888401 GARD:0017598 Oculocutaneous albinism type 5 (OCA5) is a type of oculocutaneous albinism found in one Pakistani family to date, characterized by white skin, golden hair, photophobia, nystagmus, foveal hypoplasia and impaired visual acuity, that affects males and females equally, and that has been mapped to a locus on chromosome 4q24 but whose gene has not yet been discovered. MEDGEN:854888 albinism, oculocutaneous, type V OMIM:615312 MONDO:0014127 DOID:0070099 OCA5 oculocutaneous albinism