ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 associated gene
No signs/symptoms info

Spinocerebellar ataxia with epilepsy

Recessive mitochondrial ataxia syndrome

POLG

Citations in the biomedical literature:

Spinocerebellar ataxia with epilepsy		Recessive mitochondrial ataxia syndrome
	Synonym(s): - MSCAE - Mitochondrial spinocerebellar ataxia with epilepsy - SCAE		Synonym(s): - MIRAS

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: - Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.