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

LCK CD8A


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



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

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):
- Familial CD8 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:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.