All diseases

OMIM ID
606002
OMIM term:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1
Alternative terms:
ATAXIA-OCULOMOTOR APRAXIA 2; AOA2
ATAXIA-OCULAR APRAXIA 2
(∗) Location:
9q34.13  
(†) Associated OMIM genes:
SETX  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/x7ch0z59