Showing entry for Primary hyperoxaluria type 2
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005845 |
| Disease Name | Primary hyperoxaluria type 2 |
| Disease CUI Id | C0268165 |
| MeSH Codes | C16 C18 C13 C12 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:0014667 DOID:630 |
| Disease Ontology Class Name | disease of metabolism; genetic disease |
| Disorder Network | disorder-protein-compound-food associations |
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