Selective IgM Immunodeficiency

Preferred Label : Selective IgM Immunodeficiency;

NCIt definition : A rare dysgammaglobulinemia characterized by low or undetectable serum levels of immunoglobulin class M (IgM). It is an uncommon primary antibody deficiency. It is most likely an inherited immunodeficiency. It may be caused by decreased or inefficient production of IgM from progenitor B cells without any corresponding decreases in the other isotypes. There is a widely variable clinical course. Some affected individuals may be asymptomatic while others show increased susceptibility to infection, malignancy and autoimmune disorders.;

Details

Origin ID

C26965;

UMLS CUI

C0154275;

Automatic exact mappings (from CISMeF team)
- Selective IgM immunodeficiency [ICD-9 code]
- Selective deficiency of immunoglobulin M [ICD-11 More detail]
Currated CISMeF NLP mapping
- Selective IgM deficiency [ORDO Disease]
- Selective IgM immunodeficiency [MedDRA Preferred Term]
- Selective immunoglobulin M deficiency (disorder) [SNOMED CT concept]
Semantic type(s)
- Pathologic Function [UMLS semantic type]
UMLS correspondences (same concept)
- Selective IgM deficiency [ORDO Disease]
- Selective IgM immunodeficiency [ICD-9 code]
- Selective IgM immunodeficiency [MedDRA Preferred Term]
- Selective deficiency of immunoglobulin M [IgM] [ICD-10 Sub-category]
- Selective immunoglobulin M deficiency (disorder) [SNOMED CT concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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