Showing entry for Meningomyelocele
| General Disease Information | |
|---|---|
| BXGD Id | BXGD001861 |
| Disease Name | Meningomyelocele |
| Disease CUI Id | C0025312 |
| MeSH Codes | C16 C10 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | HP:0000707 |
| Human Phenotype Ontology Term | Abnormality of the nervous system |
| Disease Ontology Id | DOID:7 DOID:0080015 |
| Disease Ontology Class Name | disease of anatomical entity; physical disorder |
| Disorder Network | disorder-protein-compound-food associations
|