ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

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

Juvenile myelomonocytic leukemia

WHIM syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PTPN11	(0.65)	CXCR4

Citations in the biomedical literature:

Juvenile myelomonocytic leukemia		WHIM syndrome
	Synonym(s): - Juvenile chronic myelomonocytic leukemia		Synonym(s): - Warts-hypogammaglobulinemia-infections-myelokathexis

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare immune disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

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

	External references: 1 OMIM reference - 1 MeSH reference: D054429		External references: 1 OMIM reference - 1 MeSH reference: C536697

No signs/symptoms info available.