Human genes for oculocutaneous albinism type III
Oculocutaneous albinism type III [DOID:0070097]
An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of TYRP1 on chromosome 9p23.
Synonyms: oculocutaneous albinism type III, DOID:0070097, oculocutaneous albinism type IIIs, OCA3, Rufous Oculocutaneous Albinism ...