Showing entry for Meningocele
| General Disease Information | |
|---|---|
| BXGD Id | BXGD001857 |
| Disease Name | Meningocele |
| Disease CUI Id | C0025299 |
| MeSH Codes | C23 C16 C05 C10 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0000707 |
| Human Phenotype Ontology Term | Abnormality of the nervous system |
| Disease Ontology Id | DOID:0080015 |
| Disease Ontology Class Name | physical disorder |
| Disorder Network | disorder-protein-compound-food associations
|