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Recessive mitochondrial ataxia syndrome
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal recessive progressive external ophthalmoplegia
1 OMIM reference -
2 associated genes
No signs/symptoms info
Recessive mitochondrial ataxia syndrome
Autosomal recessive progressive external ophthalmoplegia

POLG
(UniProt - OMIM)
 POLG
(UniProt - OMIM)
TK2
(UniProt - OMIM)

COMMON
GENES 		POLG


Citations in the biomedical literature:


Recessive mitochondrial ataxia syndrome
POLG
Autosomal recessive progressive external ophthalmoplegia
TK2



Recessive mitochondrial ataxia syndrome
Autosomal recessive progressive external ophthalmoplegia

Synonym(s):
- MIRAS
Synonym(s):
- arPEO
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):
- Diseases of the eye and adnexa -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: variable
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.