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Summary Literature (0)
MIM:203290 - ALBINISM, OCULOCUTANEOUS, TYPE III; OCA3

Xenbase Genes: tyrp1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008747 - oculocutaneous albinism type 3

Disease Ontology (DO):
DOID:0050632 - oculocutaneous albinism
DOID:0070097 - oculocutaneous albinism type III