CD8 deficiency, familial

Preferred Label : CD8 deficiency, familial;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0564124;

UMLS CUI

C1837065;

Currated CISMeF NLP mapping
- Familial CD8 deficiency [ICD-11 More detail]
- Immunodeficiency 116 [OMIM Phenotype]
- Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder) [SNOMED CT concept]
- Susceptibility to respiratory infections associated with CD8alpha chain mutation [ORDO Disease]
Related record
- CD8 deficiency, familial [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Immunodeficiency 116 [OMIM Phenotype]
- Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder) [SNOMED CT concept]
- Susceptibility to respiratory infections associated with CD8alpha chain mutation [ORDO Disease]