All diseases

OMIM ID
608029
OMIM term:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6; SCAR6
Alternative terms:
CEREBELLAR ATAXIA, INFANTILE NONPROGRESSIVE, AUTOSOMAL RECESSIVE
NORWEGIAN INFANTILE ONSET ATAXIA
(∗) Location:
20q11-q13  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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