immune deficiency, familial variable

Preferred Label : immune deficiency, familial variable;

Origin ID

C564136;

UMLS CUI

C1840266;

Currated CISMeF NLP mapping
- Immune deficiency, familial variable [OMIM Phenotype]
MeSH term(s) associated for indexing
- Primary Immunodeficiency Diseases [MeSH Descriptor]
- immunologic deficiency syndromes [MeSH Descriptor]
Record concept(s)
- immune deficiency, familial variable [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Immune deficiency, familial variable [OMIM Phenotype]