Showing entry for Properdin Deficiency, Type II
| General Disease Information | |
|---|---|
| BXGD Id | BXGD014376 |
| Disease Name | Properdin Deficiency, Type II |
| Disease CUI Id | C1839455 |
| MeSH Codes | C16 C20 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|