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Sporadic Leigh syndrome
1 OMIM reference -
3 associated genes
20 connected diseases
No signs/symptoms info
Disease Type of connection
Maternally-inherited Leigh syndrome
Leber 'plus' disease
Leber hereditary optic neuropathy
MELAS syndrome
MERRF syndrome
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Isolated NADH-CoQ reductase deficiency
Leigh syndrome with leukodystrophy
Congenital brain dysgenesis due to glutamine synthetase deficiency
Distal myopathy with posterior leg and anterior hand involvement
Early infantile epileptic encephalopathy
LIG4 syndrome
Muscle filaminopathy
Omenn syndrome
Synonym(s):
- Sporadic Leigh disease
- Sporadic infantile subacute necrotizing encephalopathy
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
MT-ND3 P03897516002
MT-ND5 P03915516005
MT-ND6 P03923516006
No signs/symptoms info available.