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Susceptibility to respiratory infections associated with CD8alpha chain mutation
1 OMIM reference -
1 associated gene
6 connected diseases
No signs/symptoms info
Disease Type of connection
Chorioretinopathy, Birdshot type
T-B+ severe combined immunodeficiency due to CD3delta / CD3epsilon / CD3zeta
Primary CD59 deficiency
T-B+ severe combined immunodeficiency due to CD45 deficiency
Severe combined immunodeficiency due to LCK deficiency
Autosomal dominant beta2-microglobulinic amyloidosis
Synonym(s):
- Familial CD8 deficiency
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 -
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
Gene symbol UniProt reference OMIM reference
CD8A P01732186910
No signs/symptoms info available.