Cytoscape Web
Click node...

Recessive mitochondrial ataxia syndrome
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Spinocerebellar ataxia with epilepsy
1 OMIM reference -
1 associated gene
No signs/symptoms info
Recessive mitochondrial ataxia syndrome
Spinocerebellar ataxia with epilepsy

POLG
(UniProt - OMIM)
 POLG
(UniProt - OMIM)

COMMON
GENES 		POLG


Citations in the biomedical literature:


Recessive mitochondrial ataxia syndrome
POLG
Spinocerebellar ataxia with epilepsy



Recessive mitochondrial ataxia syndrome
Spinocerebellar ataxia with epilepsy

Synonym(s):
- MIRAS
Synonym(s):
- MSCAE
- Mitochondrial spinocerebellar ataxia with epilepsy
- SCAE
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.