Immunodeficiencies with severe reduction in at least two serum immunoglobulin isotypes with normal or low numbers of B cells

ICD-11 code : 4A01.01;

Preferred Label : Immunodeficiencies with severe reduction in at least two serum immunoglobulin isotypes with normal or low numbers of B cells;

ICD-11 definition : This refers to a nonfamilial type of primary immune deficiency disease characterized by a reduction in at least two serum immunoglobulin isotypes. Circulating B cells may be normal or low.;

ICD-11 synonym : common variable immune deficiency; nonfamilial hypogammaglobulinaemia;

ICD-11 inclusion : hypogammaglobulinaemia antibody deficiency syndrome; Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes; acquired agammaglobulinaemia; Hypogammaglobulinaemia NOS; agammaglobulinaemia; hypogammaglobulinaemia; common variable agammaglobulinaemia; immunoglobulin-bearing b-lymphocytes agammaglobulinaemia; agammaglobulinaemia NOS; nonfamilial agammaglobulinaemia; agammaglobulinaemia antibody deficiency syndrome;

Details

Origin ID

1915135976;

Automatic exact mappings (from CISMeF team)
- Common Variable Immunodeficiency [NCIt concept]
- Common variable immunodeficiency [ORDO Disease]
- Common variable immunodeficiency [ICD-10 category]
- Common variable immunodeficiency [PASCAL descriptor]
- Immunodeficiency common variable [MedDRA Preferred Term]
- Nonfamilial hypogammaglobulinemia [ICD-10 Sub-category]
- common variable immunodeficiency [MeSH concept]
- common variable immunodeficiency [MeSH Descriptor]
ICD-10 Mapping
- Nonfamilial hypogammaglobulinemia [ICD-10 Sub-category]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients