All diseases

OMIM ID
203100
OMIM term:
ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A
Alternative terms:
OCULOCUTANEOUS ALBINISM, TYPE I; OCA1
ALBINISM I
OCULOCUTANEOUS ALBINISM, TYROSINASE-NEGATIVE; ATN
(∗) Location:
11q14.3  
(†) Associated OMIM genes:
TYR  
(‡) Associated MGI genes:
Tyr  

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