CD8 deficiency, familial

Preferred Label : CD8 deficiency, familial;

MeSH note : mutation in CD8alpha;

Origin ID

C563824;

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]
MeSH term(s) associated for indexing
- Primary Immunodeficiency Diseases [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
Record concept(s)
- CD8 deficiency, familial [MeSH 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]