Hereditary hypogammaglobulinemia

Preferred Label : Hereditary hypogammaglobulinemia;

Inclusion CIM-10 : Autosomal recessive agammaglobulinemia (Swiss type); X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency);

Diag associé à un acte (%) : 37.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D800;

UMLS CUI

C0494249;

Excluded by
- Combined immunodeficiencies [ICD-10 category]
Orphanet concepts
- Autosomal agammaglobulinemia [ORDO Disease]
- Immunodeficiency predominantly affecting antibody production [ORDO Disease]
- Isolated agammaglobulinemia [ORDO Disease]
- X-linked agammaglobulinemia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- Hereditary agammaglobulinaemia with profoundly reduced or absent B cells [ICD-11 Sub-sub category]

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