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Disease Properdin Deficiency, Type III

Name Properdin Deficiency, Type III
Categories Genetic disease (inborn) | Immune system disease
MeSH® ID C564076

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 III
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 III

Top ↑ Descendants

None.