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Spinocerebellar ataxia type 37

rare

Spinocerebellar ataxia type 37 (SCA37) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1), characterized by a cerebellar syndrome along with altered vertical eye movements.

Identifiers
MONDO:0014410 OMIM:615945Orphanet:363710
Causal genes
DAB1
Part of
Autosomal dominant cerebellar ataxia type I
Also known as
SCA37 · spinocerebellar ataxia 37 · spinocerebellar ataxia with altered vertical eye movements

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