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Disease Ontology Browser
oculocutaneous albinism type IV (DOID:0070098)
Alliance: disease page
Synonyms: OCA4
Alt IDs: OMIM:606574
Definition: An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of SLC45A2 on chromosome 5p13.2.

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