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3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Lennox-Gastaut syndrome
Idiopathic CD4 lymphocytopenia

CHD2 UNC119
MAPK10
SCN1A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MAPK10
(0.63)
UNC119



Citations in the biomedical literature:


Lennox-Gastaut syndrome
CHD2 MAPK10 SCN1A
Idiopathic CD4 lymphocytopenia
UNC119



Lennox-Gastaut syndrome
Idiopathic CD4 lymphocytopenia

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)

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: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic

External references:
No OMIM references
1 MeSH reference: C535500
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.