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Susceptibility to respiratory infections associated with CD8alpha chain mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Severe combined immunodeficiency due to LCK deficiency
1 associated gene
No signs/symptoms info
Susceptibility to respiratory infections associated with CD8alpha chain mutation
Severe combined immunodeficiency due to LCK deficiency

CD8A
(UniProt - OMIM)
 LCK
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CD8A
(0.59)
LCK


Citations in the biomedical literature:


Susceptibility to respiratory infections associated with CD8alpha chain mutation
CD8A
Severe combined immunodeficiency due to LCK deficiency
LCK



Susceptibility to respiratory infections associated with CD8alpha chain mutation
Severe combined immunodeficiency due to LCK deficiency

Synonym(s):
- Familial CD8 deficiency
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 genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune 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: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.