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Primary Immunodeficiency Diseases MeSH Descriptor Data 2023


MeSH Heading
Primary Immunodeficiency Diseases
Tree Number(s)
C16.320.798
C20.673.795
Unique ID
D000081207
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000081207
Scope Note
Genetic immunologic deficiency diseases and syndromes due to mutations in genes involved in IMMUNITY generally characterized by an increased susceptibility to infectious diseases. They are often associated with AUTOIMMUNE DISEASE manifestations.
Entry Term(s)
Congenital Immunodeficiency Disease
Congenital Immunodeficiency Diseases
Congenital Immunodeficiency Disorder
Congenital Immunodeficiency Disorders
Congenital Immunodeficiency Syndrome
Congenital Immunodeficiency Syndromes
Inherited Immunodeficiency Disease
Inherited Immunodeficiency Diseases
Inherited Immunodeficiency Disorder
Inherited Immunodeficiency Disorders
Inherited Immunodeficiency Syndrome
Inherited Immunodeficiency Syndromes
Primary Antibody Deficiencies
Primary Antibody Deficiency Disorder
Primary Antibody Deficiency Disorders
Primary Antibody Deficiency Syndrome
Primary Antibody Deficiency Syndromes
Primary Immune Deficiency
Primary Immune Deficiency Disease
Primary Immune Deficiency Diseases
Primary Immune Deficiency Disorder
Primary Immune Deficiency Disorders
Primary Immune Deficiency Syndrome
Primary Immune Deficiency Syndromes
Primary Immunodeficiency Disease
Primary Immunodeficiency Disorder
Primary Immunodeficiency Disorders
Primary Immunodeficiency Syndromes
Previous Indexing
Immunologic Deficiency Syndromes (1972-2019)
Public MeSH Note
2020
History Note
2020
Date Established
2020/01/01
Date of Entry
2019/07/08
Revision Date
2020/05/27
Primary Immunodeficiency Diseases Preferred
Congenital Immunodeficiency Diseases Narrower
Inherited Immunodeficiency Diseases Narrower
Primary Antibody Deficiencies Narrower
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