OBO ID: DOID:626 |
Term Name: | complement deficiency | Search Ontology: | |
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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. http://en.wikipedia.org/wiki/Complement_deficiency | ||
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Ontology: | Human Disease ( DOID:626 ) |
OTHER complement deficiency PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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