Showing entry for Epilepsy, Familial Temporal Lobe 1
| General Disease Information | |
|---|---|
| BXGD Id | BXGD023448 |
| Disease Name | Epilepsy, Familial Temporal Lobe 1 |
| Disease CUI Id | C4551957 |
| MeSH Codes | C23 C10 F03 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 DOID:7 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations
|