Familial Adult Myoclonic Epilepsy
Disease ID: disease_node_16282
Connections displayed (default: 10).
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| Dbxref | MIM:PS601068, ORDO:86814, SNOMEDCT_US_2023_03_01:717225001, UMLS_CUI:C4273988 |
|---|---|
| Subclassof | DOID_0050705 |
| Data Source | DOID |
| Synonyms | BAFME, FAME, FCMTE, benign adult familial myoclonic epilepsy, benign adult familial myoclonus epilepsy, familial cortical myoclonic tremor and epilepsy |
| Doid Label | familial adult myoclonic epilepsy |
| Doid Description | An adolescence-adult electroclinical syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities. |
| Existence Starts During | HP_0003581 |
| Disease Node Id | disease_node_16282 |
| Doid Id | DOID_0111689 |
| Label | Familial Adult Myoclonic Epilepsy |
- Incoming r'ship
SUBCLASS_OFto/from Familial Adult Myoclonic Epilepsy 1(ID:disease_node_16289) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Adult Myoclonic Epilepsy 6(ID:disease_node_16283) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Adult Myoclonic Epilepsy 2(ID:disease_node_16287) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Adult Myoclonic Epilepsy 7(ID:disease_node_16285) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Adult Myoclonic Epilepsy 5(ID:disease_node_16288) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Adult Myoclonic Epilepsy 4(ID:disease_node_16286) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Adolescence-Adult Electroclinical Syndrome(ID:disease_node_16275) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Adult Myoclonic Epilepsy 3(ID:disease_node_16284) (Disease)