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MIM:606952 - ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B
Echinobase Genes:
Human Disease Resource: MIM
DOID:0050632 - oculocutaneous albinism |
DOID:0070095 - oculocutaneous albinism type IB |
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DOID:0050632 - oculocutaneous albinism |
DOID:0070095 - oculocutaneous albinism type IB |