Benign Familial Infantile Seizures 2
Disease ID: disease_node_16311
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:605751 |
|---|---|
| Subclassof | DOID_0050736, DOID_0060169 |
| Data Source | DOID |
| Synonyms | Benign Familial Infantile Seizures, 2 |
| Doid Label | benign familial infantile seizures 2 |
| Doid Description | A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in mutation in the PRRT2 gene on chromosome 16p11. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16311 |
| Doid Id | DOID_0081115 |
| Label | Benign Familial Infantile Seizures 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Benign Familial Infantile Epilepsy(ID:disease_node_16306) (Disease)