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Summary Literature (1)
MIM:203100 - ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A

Xenbase Genes: tyr

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008745 - oculocutaneous albinism type 1A
MONDO:0018135 - oculocutaneous albinism type 1

Disease Ontology (DO):
DOID:0050632 - oculocutaneous albinism
DOID:0070094 - oculocutaneous albinism type IA