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Disease Ontology Browser
oculocutaneous albinism type II (DOID:0070096)
Alliance: disease page
Synonyms: OCA2; Oculocutaneous Albinism, Tyrosinase-Positive
Alt IDs: OMIM:203200
Definition: An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.14
The Jackson Laboratory