Showing entry for Neonatal Jaundice
| General Disease Information | |
|---|---|
| BXGD Id | BXGD001539 |
| Disease Name | Neonatal Jaundice |
| Disease CUI Id | C0022353 |
| MeSH Codes | C23 C16 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0025031 HP:0001574 |
| Human Phenotype Ontology Term | Abnormality of the digestive system; Abnormality of the integument |
| Disease Ontology Id | DOID:7 |
| Disease Ontology Class Name | disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations
|