Familial Temporal Lobe Epilepsy 3
Disease ID: disease_node_13373
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:611630, ORDO:163717 |
|---|---|
| Subclassof | DOID_0050736, DOID_3328 |
| Data Source | DOID |
| Synonyms | FMTLE, familial mesial temporal lobe epilepsy |
| Doid Label | familial temporal lobe epilepsy 3 |
| Doid Description | A temporal lobe epilepsy characterized by simple or complex partial seizures often accompanied by intense feelings of deja or altered awareness and that has_material_basis_in variation in the chromosome region 4q13.2-q21.3. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_13373 |
| Doid Id | DOID_0060750 |
| Label | Familial Temporal Lobe Epilepsy 3 |
- Outgoing r'ship
SUBCLASS_OFto/from Epilepsy, Temporal Lobe(ID:disease_node_2984) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)