Term Name:	oculocutaneous albinism type II
Synonyms:	OCA2, Oculocutaneous Albinism, Tyrosinase-Positive
Definition:	An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the OCA2 gene on chromosome 15q12-q13.
Ontology:	Human Disease [DOID:0070096]   ( DOID:0070096 )