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Disease Properdin deficiency, X-linked

Name Properdin deficiency, X-linked
Synonyms CFPD | COMPLEMENT FACTOR PROPERDIN DEFICIENCY | PFD | Properdin deficiency, type 1 | Properdin Deficiency, Type I | PROPERDIN DEFICIENCY, TYPE III, INCLUDED | PROPERDIN DEFICIENCY, TYPE I PROPERDIN DEFICIENCY, TYPE II, INCLUDED | Properdin P factor deficiency
Categories Genetic disease (inborn)
MeSH® ID C537241
OMIM® ID 312060

Top ↑ Ancestors

DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, X-Linked Has associated chemicals Has associated genes Properdin deficiency, X-linked Has associated chemicals Has associated genes

Top ↑ Descendants

None.