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Recessive mitochondrial ataxia syndrome
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant progressive external ophthalmoplegia
Alpers syndrome
Autosomal recessive progressive external ophthalmoplegia
Mitochondrial neurogastrointestinal encephalomyopathy
Sensory ataxic neuropathy - dysarthria - ophthalmoparesis
Spinocerebellar ataxia with epilepsy
Burkitt lymphoma
Precursor T-cell acute lymphoblastic leukemia
Synonym(s):
- MIRAS
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
POLG P54098174763
No signs/symptoms info available.