Showing entry for Alagille Syndrome
| General Disease Information | |
|---|---|
| BXGD Id | BXGD003151 |
| Disease Name | Alagille Syndrome |
| Disease CUI Id | C0085280 |
| MeSH Codes | C16 C06 C14 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:7 |
| Disease Ontology Class Name | disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations
|