Properdin deficiency
From Infogalactic: the planetary knowledge core
Properdin deficiency | |
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Classification and external resources | |
Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
OMIM | 312060 |
Patient UK | Properdin deficiency |
Properdin deficiency is a rare X-linked disease in which properdin, an important complement factor, is deficient.[1] Affected individuals are susceptible to fulminant meningococcal disease.
References
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