All diseases

OMIM ID
214450
OMIM term:
GRISCELLI SYNDROME, TYPE 1; GS1
Alternative terms:
GRISCELLI SYNDROME WITH NEUROLOGIC IMPAIRMENT
PARTIAL ALBINISM AND PRIMARY NEUROLOGIC DISEASE WITHOUT HEMOPHAGOCYTIC SYNDROME
GRISCELLI SYNDROME, CUTANEOUS AND NEUROLOGIC TYPE
(∗) Location:
15q21.2  
(†) Associated OMIM genes:
MYO5A  
(‡) Associated MGI genes:
Myo5a  

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