Showing entry for Encephalocele
| General Disease Information | |
|---|---|
| BXGD Id | BXGD023402 |
| Disease Name | Encephalocele |
| Disease CUI Id | C4551722 |
| MeSH Codes | C23 C16 C13 C10 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Nervous System Diseases |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | HP:0000707 HP:0000152 HP:0000924 |
| Human Phenotype Ontology Term | Abnormality of the nervous system; Abnormality of head or neck; Abnormality of the skeletal system |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|