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| Term | complement deficiency | ID (Ontology) | DOID:626 (Human Disease) |
| Definition | A 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. | ||
| Also Known As | "Complement deficiency disease" | ||
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| Is a | primary immunodeficiency disease | ||
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External Crossreferences & Linkouts
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ICD10CM:D84.1 MESH:D000081208 NCI:C4691 SNOMEDCT_US_2023_03_01:191014008 UMLS_CUI:C0272242 |
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