Human genes for oculocutaneous albinism type V
Oculocutaneous albinism type V [DOID:0070099]
An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of OCA5 on chromosome 4q24.
Synonyms: oculocutaneous albinism type V, DOID:0070099, oculocutaneous albinism type Vs, OCA5