ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 3

3 OMIM references -
5 associated genes
No signs/symptoms info

Severe combined immunodeficiency due to LCK deficiency

Autoimmune lymphoproliferative syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LCK LCK LCK	(0.85) (0.75) (0.52)	FAS FASLG PRKCD

Citations in the biomedical literature:

Severe combined immunodeficiency due to LCK deficiency		Autoimmune lymphoproliferative syndrome
	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): - ALPS - Canale-Smith syndrome - FAS deficiency

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

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

	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: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 3 OMIM references - 1 MeSH reference: D056735

No signs/symptoms info available.