ODCs

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1 OMIM reference -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

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

Juvenile myelomonocytic leukemia

Multiple endocrine neoplasia type 2A


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CBL PTPN11	(0.87) (0.52)	RET RET

Citations in the biomedical literature:

Juvenile myelomonocytic leukemia		Multiple endocrine neoplasia type 2A
	Synonym(s): - Juvenile chronic myelomonocytic leukemia		Synonym(s): - MEN2A - PTC syndrome - Sipple syndrome

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare endocrine disease - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Neoplasms -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D054429		External references: 1 OMIM reference - 1 MeSH reference: D018813

No signs/symptoms info available.