Selective IgD Immunodeficiency

Preferred Label : Selective IgD Immunodeficiency;

NCIt definition : A rare dysgammaglobulinemia characterized by low or undetectable serum levels of immunoglobulin class D (IgD). It is an uncommon primary antibody deficiency. It is most likely an inherited immunodeficiency. It may be caused by decreased or inefficient production of IgD from progenitor B cells without any corresponding decreases in the other isotypes. Most affected persons are asymptomatic and do not appear to be at increased risk for infection.;

Détails

Origin ID

C27144;

UMLS CUI

C0398695;

Automatic exact mappings (from CISMeF team)
- selective IgD deficiency disease [DO Concept]
CISMeF manual mappings
- Selective immunoglobulin D deficiency (disorder) [SNOMED CT concept]
DO Cross reference
- selective IgD deficiency disease [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Selective immunoglobulin D deficiency (disorder) [SNOMED CT concept]
- selective IgD deficiency disease [DO Concept]
disease_has_primary_anatomic_site
- Immune System [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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