Spinocerebellar ataxia type 25

Disease Export to PDF
Name:
Spinocerebellar ataxia type 25
Description:
Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by cerebellar ataxia and prominent sensory neuropathy.
ORPHAcode:
101111
Synonyms:
SCA25
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14