Details of Disease

General Information of Disease (ID: DISBK94W)

Disease Name Spinocerebellar ataxia type 26
Synonyms spinocerebellar ataxia 26; spinocerebellar ataxia type 26; SCA26
Definition
Spinocerebellar ataxia type 26 (SCA26) is a very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities.
Disease Hierarchy
DISQBYEM: Autosomal dominant cerebellar ataxia type III
DISBK94W: Spinocerebellar ataxia type 26
Disease Identifiers
MONDO ID
MONDO_0012246
MESH ID
C537203
UMLS CUI
C1836395
OMIM ID
609306
MedGen ID
373077
Orphanet ID
101112
SNOMED CT ID
718769009

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
EEF2 OTZ7SZ39 Strong Autosomal dominant [1]
------------------------------------------------------------------------------------

References

1 Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6. Ann Neurol. 2005 Mar;57(3):349-54. doi: 10.1002/ana.20371.