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Disease Ontology Browser
oculocutaneous albinism (DOID:0050632)
Alliance: disease page
Alt IDs: OMIM:203100, OMIM:203200, OMIM:203290, OMIM:606574, OMIM:606952, OMIM:614473, OMIM:615312, ICD10CM:E70.3, MESH:D016115, ORDO:55
Definition: An autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes.

Disease References using Mouse Models (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.13
The Jackson Laboratory