complement deficiency
(Q5156409)
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
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
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Current Data About
complement deficiency
| (P31) |
(Q112193867)
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| (P279) |
(Q3043160)
(Q2351083)
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| (P373) |
Complement deficiencies
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| (P689) |
(Q334848)
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| (P910) |
(Q8405549)
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| (P1692) |
279.8
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| (P1748) |
C4691
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| (P1995) |
(Q103824)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_626
http://identifiers.org/doid/DOID:626
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| (P5008) |
(Q4099686)
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other details
| aliases |
Complement deficiency disease (disorder) Complement deficiency Complement deficiency disease disorder of complement activation |
| description | 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 |
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