Showing entry for Infant, Premature, Diseases
| General Disease Information | |
|---|---|
| BXGD Id | BXGD001492 |
| Disease Name | Infant, Premature, Diseases |
| Disease CUI Id | C0021295 |
| MeSH Codes | C16 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|