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Severe combined immunodeficiency due to LCK deficiency
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
1 associated gene
No signs/symptoms info
Severe combined immunodeficiency due to LCK deficiency
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia

LCK
(UniProt - OMIM)
 PIK3CA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LCK
(0.89)
PIK3CA


Citations in the biomedical literature:


Severe combined immunodeficiency due to LCK deficiency
LCK
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
PIK3CA



Severe combined immunodeficiency due to LCK deficiency
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia

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 developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)
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:
No OMIM references
No MeSH references
No signs/symptoms info available.