loading...| Preferred Name | Myoclonic Epilepsies, Progressive [Disease/Finding] | |
| Synonyms |
Progressive Myoclonus Epilepsies Myoclonic Epilepsies, Progressive Myoclonic Epilepsy, Progressive Progressive Myoclonic Epilepsy |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000004030 |
|
| altLabel |
Progressive Myoclonus Epilepsies Myoclonic Epilepsies, Progressive Myoclonic Epilepsy, Progressive Progressive Myoclonic Epilepsy |
|
| cui |
C0751778 |
|
| MESH DEFINITION |
A heterogeneous group of primarily familial disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intellectual deterioration, and neuronal degeneration. These include LAFORA DISEASE; MERRF SYNDROME; NEURONAL CEROID-LIPOFUSCINOSIS; sialidosis (see MUCOLIPIDOSES), and UNVERRICHT-LUNDBORG SYNDROME. |
|
| MESH DUI |
D020191 |
|
| MeSH name |
Myoclonic Epilepsies, Progressive |
|
| MESH UI |
M0328687 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000004030 |
|
| NUI |
N0000004030 |
|
| prefLabel |
Myoclonic Epilepsies, Progressive [Disease/Finding] |
|
| SNOMED CID |
267581004 |
|
| tui |
T047 |
|
| subClassOf |