补体缺陷病
Sign in to saveAlso known as Complement deficiency disease (disorder), Complement deficiency, Complement deficiency disease, disorder of complement activation
primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation
Wikidata facts
- Subclass of
- metabolic disease
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- NCI Thesaurus ID
- C4691
- health specialty
- hematology
- afflicts
- complement system
- exact match
- identifiers.org/doid/DOID:626
- Commons category
- Complement deficiencies
- ICD-9-CM
- 279.8
- on focus list of Wikimedia project
- WikiProject Medicine
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