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| Term | C1 inhibitor deficiency | ID (Ontology) | DOID:0060002 (Human Disease) |
| Definition | A complement deficiency that is a functional deficiency in the complement component C1 inhibitor leading to hereditary angioedema (HAE) involving swelling due to leakage of fluid from blood vessels into connective tissue." [url:http\://en.wikipedia.org/wiki/C1-inhibitor#Role_in_disease] {comment="ls:IEDB"} | ||
| Also Known As | "Quincke edema" | ||
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primary immunodeficiency disease |__complement deficiency |__C1 inhibitor deficiency |
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| Is a | complement deficiency | ||
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