ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

3 associated genes
No signs/symptoms info

Multiple endocrine neoplasia type 4

Lennox-Gastaut syndrome


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

Citations in the biomedical literature:

Multiple endocrine neoplasia type 4		Lennox-Gastaut syndrome
	Synonym(s): - MEN4		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.