ODCs

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1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

Severe combined immunodeficiency due to LCK deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KIT	(0.88)	LCK

Citations in the biomedical literature:

Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease		Severe combined immunodeficiency due to LCK deficiency
	Synonym(s): (no synonyms)		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

	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: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
	Very frequent - Acute leukemia - Eosinophils anomalies / hypereosinophilia - Mastocytosis - Myeloproliferative syndrome / chronic leukemia
Severe combined immunodeficiency due to LCK deficiency
(no data available)