All diseases

OMIM ID
608687
OMIM term:
SPINOCEREBELLAR ATAXIA 20; SCA20
Alternative terms:
CHROMOSOME 11q12 DUPLICATION SYNDROME, 260-KB
SPINOCEREBELLAR ATAXIA WITH DYSPHONIA
SPINOCEREBELLAR ATAXIA WITH SPASMODIC COUGH
(∗) Location:
11q12  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/uqqdxmq8