hypogammaglobulinemia, X-Linked

Preferred Label : hypogammaglobulinemia, X-Linked;

MeSH note : mutation in Bruton tyrosine kinase;

Origin ID

C562478;

UMLS CUI

C0241932;

Automatic exact mappings (from CISMeF team)
- Agammaglobulinemia, X-linked [OMIM Phenotype]
Currated CISMeF NLP mapping
- X-linked hypogammaglobulinemia (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- agammaglobulinemia [MeSH Descriptor]
- genetic diseases, X-linked [MeSH Descriptor]
Record concept(s)
- hypogammaglobulinemia, X-Linked [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- X-linked hypogammaglobulinemia (disorder) [SNOMED CT concept]