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Maternally-inherited spastic paraplegia
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
NARP syndrome
Fanconi anemia
Acyl-CoA dehydrogenase 9 deficiency
Isolated NADH-CoQ reductase deficiency
Synonym(s):
- Maternally-inherited SPG
Classification (Orphanet):
- 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
MT-ATP6 P00846516060
No signs/symptoms info available.