Structured Summary
Abstract
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.
MeSH Record
Classification
Broader headings
Related Concepts
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MeSH Record
Synonyms
54 entry terms
- 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
- Deficiency, Primary Immune
- Immune Deficiency, Primary
- Immunodeficiency Disease, Primary
- Immunodeficiency Diseases, Primary
- Immunodeficiency Disorder, Primary
- Immunodeficiency Syndrome, Primary
- Immunodeficiency Syndromes, Primary
- Primary Immune Deficiencies
- Primary Immunodeficiency Syndrome
- Congenital Immunodeficiency Disease
- Congenital Immunodeficiency Diseases
- Congenital Immunodeficiency Disorder
- Congenital Immunodeficiency Disorders
- Congenital Immunodeficiency Syndrome
- Congenital Immunodeficiency Syndromes
- Inborn Error of Immunity
- Inborn Error of Immunity (IEI)
- Inborn Errors of Immunity
- Inherited Immunodeficiency Disease
- Inherited Immunodeficiency Diseases
- Inherited Immunodeficiency Disorder
- Inherited Immunodeficiency Disorders
- Inherited Immunodeficiency Syndromes
- Primary Antibody Deficiencies
- Primary Antibody Deficiency Disorder
- Primary Antibody Deficiency Disorders
- Primary Antibody Deficiency Syndrome
- Primary Antibody Deficiency Syndromes
- Antibody Deficiency, Primary
- Immunodeficiency Disease, Congenital
- Immunodeficiency Disease, Inherited
- Immunodeficiency Diseases, Congenital
- Immunodeficiency Diseases, Inherited
- Immunodeficiency Disorder, Congenital
- Immunodeficiency Disorder, Inherited
- Immunodeficiency Disorders, Congenital
- Immunodeficiency Disorders, Inherited
- Immunodeficiency Syndrome, Congenital
- Immunodeficiency Syndrome, Inherited
- Immunodeficiency Syndromes, Congenital
- Immunodeficiency Syndromes, Inherited
- Inherited Immunodeficiency Syndrome
- Primary Antibody Deficiency
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2020
MeSH Record
Previous Indexing
- Immunologic Deficiency Syndromes (1972-2019)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Primary Immunodeficiency Diseases. Medical Subject Headings (MeSH). 2026. Unique ID D000081207. http://id.nlm.nih.gov/mesh/2026/D000081207
- Primary Immunodeficiency Diseases. In: Wikipedia. https://en.wikipedia.org/wiki/Primary_immunodeficiency
- Primary Immunodeficiency Diseases. In: Wikidata. https://www.wikidata.org/wiki/Q3043160