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NARP syndrome
1 OMIM reference -
1 associated gene
7 connected diseases
No signs/symptoms info
Disease Type of connection
Familial infantile bilateral striatal necrosis
Leber hereditary optic neuropathy
Maternally-inherited Leigh syndrome
Maternally-inherited spastic paraplegia
Fanconi anemia
Acyl-CoA dehydrogenase 9 deficiency
Isolated NADH-CoQ reductase deficiency
Synonym(s):
- Neurogenic muscle weakness - ataxia - retinitis pigmentosa
- Neuropathy - ataxia - retinitis pigmentosa
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: childhood
Average age of death: adult
Type of inheritance: mitochondrial inheritance
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
MT-ATP6 P00846516060
No signs/symptoms info available.