Familial Focal Epilepsy With Variable Foci
Disease ID: disease_node_13377
Connections displayed (default: 10).
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| Dbxref | GARD:13295, MIM:PS604364, ORDO:98820 |
|---|---|
| Subclassof | DOID_0050736, DOID_2234 |
| Data Source | DOID |
| Synonyms | DEPDC5-related epilepsy |
| Doid Label | familial focal epilepsy with variable foci |
| Doid Description | A focal epilepsy that is characterized by focal seizures, with seizure onset in a discrete area of the brain including the temporal, frontal, parietal, and occipital lobes, with focal seizures arising from different cortical regions in different family members. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_13377 |
| Doid Id | DOID_0081420 |
| Label | Familial Focal Epilepsy With Variable Foci |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Focal Epilepsy With Variable Foci 2(ID:disease_node_13380) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Focal Epilepsy With Variable Foci 4(ID:disease_node_13378) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Focal Epilepsy With Variable Foci 1(ID:disease_node_13381) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Epilepsies, Partial(ID:disease_node_2977) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Focal Epilepsy With Variable Foci 3(ID:disease_node_13379) (Disease)