Showing entry for 17,20-Lyase Deficiency, Isolated
| General Disease Information | |
|---|---|
| BXGD Id | BXGD018723 |
| Disease Name | 17,20-Lyase Deficiency, Isolated |
| Disease CUI Id | C3277849 |
| MeSH Codes | C16 C18 C13 C12 C19 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System 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
|