Structured Summary
Abstract
Genetic disorders due to mutations in genes involved in COMPLEMENT SYSTEM PROTEINS. They are often classified into distinct pathway of complement activation where causative mutations are found (e.g., classical pathway, lectin pathway, alternative pathway, and terminal complement pathway).
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Classification
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Synonyms
3 entry terms
- Inherited Complement Deficiency Diseases
- Complement Deficiencies
- Complement Deficiency
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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
- Complement System Proteins (1971-2019)
- Immunologic Deficiency Syndromes (1971-2019)
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AMA Style
References
- National Library of Medicine. Hereditary Complement Deficiency Diseases. Medical Subject Headings (MeSH). 2026. Unique ID D000081208. http://id.nlm.nih.gov/mesh/2026/D000081208
- Hereditary Complement Deficiency Diseases. In: Wikidata. https://www.wikidata.org/wiki/Q98815014