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Summary Literature (0)
MIM:203200 - ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2

Xenbase Genes: mc1r, oca2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008746 - oculocutaneous albinism type 2

Disease Ontology (DO):
DOID:0050632 - oculocutaneous albinism
DOID:0070096 - oculocutaneous albinism type II