Showing entry for Hepatic Fibrosis, Congenital
| General Disease Information | |
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| BXGD Id | BXGD000624 |
| Disease Name | Hepatic Fibrosis, Congenital |
| Disease CUI Id | C0009714 |
| MeSH Codes | C23 C16 C06 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0025031 |
| Human Phenotype Ontology Term | Abnormality of the digestive system |
| Disease Ontology Id | DOID:630 DOID:7 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations |
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