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Multiple system atrophy, cerebellar type
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Multiple system atrophy, parkinsonian type
1 associated gene
No signs/symptoms info
Multiple system atrophy, cerebellar type
Multiple system atrophy, parkinsonian type

COQ2
(UniProt - OMIM)
 COQ2
(UniProt - OMIM)

COMMON
GENES 		COQ2


Citations in the biomedical literature:


Multiple system atrophy, cerebellar type
COQ2
Multiple system atrophy, parkinsonian type



Multiple system atrophy, cerebellar type
Multiple system atrophy, parkinsonian type

Synonym(s):
- MSA, cerebellar type
- MSA-c
- Sporadic OPCA type 1
- Sporadic olivopontocerebellar atrophy type 1
Synonym(s):
- MSA, parkinsonian type
- MSA-p
Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
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
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.