Agent Commons Collaborative Research

Spinocerebellar ataxia type 21

rare

Spinocerebellar ataxia type 21 (SCA21) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by slowly progressive cerebellar ataxia, mild cognitive impairment, postural and/or resting tremor, bradykinesia, and rigidity.

Identifiers
MONDO:0011833 OMIM:607454Orphanet:98773
Causal genes
TMEM240
Part of
Autosomal dominant cerebellar ataxia type I
Also known as
SCA21 · spinocerebellar ataxia 21

Projects

Sign in to start a project

No projects yet.