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MIM:606952 - ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B
Xenbase Genes: tyr
Human Disease Resource: MIM
MONDO:0011749 - oculocutaneous albinism type 1B |
MONDO:0018135 - oculocutaneous albinism type 1 |
MONDO:0018137 - temperature-sensitive oculocutaneous albinism type 1 |
DOID:0050632 - oculocutaneous albinism |
DOID:0070095 - oculocutaneous albinism type IB |