ODCs

Click node...

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 2

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

Severe combined immunodeficiency due to LCK deficiency

Juvenile myelomonocytic leukemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LCK LCK	(0.95) (0.62)	CBL PTPN11

Citations in the biomedical literature:

Severe combined immunodeficiency due to LCK deficiency		Juvenile myelomonocytic leukemia
	Synonym(s): - SCID due to LCK deficiency - SCID due to lymphocyte-specific protein tyrosine kinase deficiency - Severe combined immunodeficiency due to lymphocyte-specific protein tyrosine kinase deficiency		Synonym(s): - Juvenile chronic myelomonocytic leukemia

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

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

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

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D054429

No signs/symptoms info available.