Showing entry for Hereditary Coproporphyria
| General Disease Information | |
|---|---|
| BXGD Id | BXGD003950 |
| Disease Name | Hereditary Coproporphyria |
| Disease CUI Id | C0162531 |
| MeSH Codes | C16 C06 C18 C17 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue 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
|