Properdin deficiency

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Properdin deficiency
Classification and external resources
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OMIM 312060
Patient UK Properdin deficiency
[[[d:Lua error in Module:Wikidata at line 863: attempt to index field 'wikibase' (a nil value).|edit on Wikidata]]]

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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