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MIM:203200 - ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2
Xenbase Genes: mc1r, oca2
Human Disease Resource: MIM
MONDO:0008746 - oculocutaneous albinism type 2 |
DOID:0050632 - oculocutaneous albinism |
DOID:0070096 - oculocutaneous albinism type II |
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MONDO:0008746 - oculocutaneous albinism type 2 |
DOID:0050632 - oculocutaneous albinism |
DOID:0070096 - oculocutaneous albinism type II |