Nonfamilial hypogammaglobulinemia

Preferred Label : Nonfamilial hypogammaglobulinemia;

Inclusion CIM-10 : Common variable agammaglobulinemia [CVAgamma]; Hypogammaglobulinemia NOS; Agammaglobulinemia with immunoglobulin-bearing B-lymphocytes;

Diag associé à un acte (%) : 37.1;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D801;

UMLS CUI

C0494250;

Automatic exact mappings (from CISMeF team)
- Immunodeficiencies with severe reduction in at least two serum immunoglobulin isotypes with normal or low numbers of B cells [ICD-11 Sub-sub category]
DO Cross reference
- agammaglobulinemia [DO Concept]
Orphanet concepts
- Immunodeficiency predominantly affecting antibody production [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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