All diseases

OMIM ID
203200
OMIM term:
ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2
Alternative terms:
OCULOCUTANEOUS ALBINISM, TYPE II
OCULOCUTANEOUS ALBINISM, TYROSINASE-POSITIVE
ALBINISM II ALBINISM, BROWN OCULOCUTANEOUS, INCLUDED; BOCA, INCLUDED
BROWN OCULOCUTANEOUS ALBINISM, INCLUDED
(∗) Location:
15q12-q13   16q24.3  
(†) Associated OMIM genes:
MC1R   OCA2 GENE  
(‡) Associated MGI genes:

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