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Lennox-Gastaut syndrome
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
1 OMIM reference -
2 associated genes
No signs/symptoms info
Lennox-Gastaut syndrome
Amyotrophic lateral sclerosis-parkinsonism-dementia complex

CHD2
(UniProt - OMIM)
 PARK7
(UniProt - OMIM)
MAPK10
(UniProt - OMIM)
 TRPM7
(UniProt - OMIM)
SCN1A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CHD2
(0.63)
PARK7


Citations in the biomedical literature:


Lennox-Gastaut syndrome
CHD2 MAPK10 SCN1A
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
PARK7 TRPM7



Lennox-Gastaut syndrome
Amyotrophic lateral sclerosis-parkinsonism-dementia complex

Synonym(s):
(no synonyms)

Synonym(s):
- Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam
- Guam disease
- Lytico-Bodig disease
- PDALS
- Parkinsonism-dementia-ALS complex
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: C535500
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.