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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
Multiple endocrine neoplasia type 4

CHD2 CDKN1B
MAPK10
SCN1A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MAPK10
(0.56)
CDKN1B



Citations in the biomedical literature:


Lennox-Gastaut syndrome
CHD2 MAPK10 SCN1A
Multiple endocrine neoplasia type 4
CDKN1B



Lennox-Gastaut syndrome
Multiple endocrine neoplasia type 4

Synonym(s):
(no synonyms)

Synonym(s):
- MEN4

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -

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: -
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.