agammaglobulinemia, non-Bruton type

Preferred Label : agammaglobulinemia, non-Bruton type;

MeSH synonym : agammaglobulinemia due to early proB cell defect; agammaglobulinemia, autosomal recessive; agammaglobulinemia, Non-Bruton type, autosomal recessive;

Details

Origin ID

C538056;

UMLS CUI

C1832241;

CISMeF manual mappings
- Autosomal agammaglobulinemia [ORDO Disease]
Currated CISMeF NLP mapping
- Agammaglobulinemia 1, autosomal recessive [OMIM Phenotype]
- Autosomal Recessive Agammaglobulinemia [NCIt concept]
- Autosomal recessive agammaglobulinaemia [ICD-11 More detail]
False automatic mappings
- X-linked agammaglobulinemia (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- agammaglobulinemia [MeSH Descriptor]
Record concept(s)
- Agammaglobulinemia, non-Bruton type [MeSH concept]
See also inter- (CISMeF)
- X-linked agammaglobulinemia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal agammaglobulinemia [ORDO Disease]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients