Human genes for oculocutaneous albinism type VII
Oculocutaneous albinism type VII [DOID:0070100]
An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of C10orf11 on chromosome 10q22.2-q22.3.
Synonyms: oculocutaneous albinism type VII, DOID:0070100, oculocutaneous albinism type VIIs, OCA7