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Multiple system atrophy, cerebellar type
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
Leigh syndrome with nephrotic syndrome
Multiple system atrophy, parkinsonian type
Synonym(s):
- MSA, cerebellar type
- MSA-c
- Sporadic OPCA type 1
- Sporadic olivopontocerebellar atrophy type 1
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
COQ2 Q96H96609825
No signs/symptoms info available.