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Severe combined immunodeficiency due to LCK deficiency
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hepatocellular carcinoma, childhood-onset
2 associated genes
No signs/symptoms info
Severe combined immunodeficiency due to LCK deficiency
Hepatocellular carcinoma, childhood-onset

LCK
(UniProt - OMIM)
 CTNNB1
(UniProt - OMIM)
MET
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LCK
(0.72)
MET


Citations in the biomedical literature:


Severe combined immunodeficiency due to LCK deficiency
LCK
Hepatocellular carcinoma, childhood-onset
CTNNB1 MET



Severe combined immunodeficiency due to LCK deficiency
Hepatocellular carcinoma, childhood-onset

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):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare hepatic 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:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.