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Disease Properdin Deficiency, Type II

Name Properdin Deficiency, Type II
Categories Genetic disease (inborn) | Immune system disease
MeSH® ID C564075

Top ↑ Ancestors

1. 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, Type II
2. DiseasesImmune System Diseases Has associated chemicals Has associated genes Has associated exposure references Immunologic Deficiency Syndromes Has associated chemicals Has associated genes Properdin Deficiency, Type II

Top ↑ Descendants

None.