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Lennox-Gastaut syndrome
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Kostmann syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Lennox-Gastaut syndrome
Kostmann syndrome

CHD2
(UniProt - OMIM)
 HAX1
(UniProt - OMIM)
MAPK10
(UniProt - OMIM)
SCN1A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MAPK10
(0.86)
HAX1


Citations in the biomedical literature:


Lennox-Gastaut syndrome
CHD2 MAPK10 SCN1A
Kostmann syndrome
HAX1



Lennox-Gastaut syndrome
Kostmann syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
1 MeSH reference: C535500
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.