loading...| Preferred Name | Progressive Myoclonic Epilepsy | |
| Synonyms |
|
|
| Definitions |
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). |
|
| ID |
http://uri.neuinfo.org/nif/nifstd/birnlex_12722 |
|
| createdDate |
2007-10-08 |
|
| 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). |
|
| editorial note | ||
| externalSourceId |
D020191 |
|
| hasBirnlexCurator | ||
| hasCurationStatus | ||
| hasDefinitionSource | ||
| hasExternalSource | ||
| label |
Progressive Myoclonic Epilepsy |
|
| MeshUid |
D020191 |
|
| modifiedDate |
2007-10-08 |
|
| note |
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). |
|
| preferred label |
Progressive Myoclonic Epilepsy |
|
| putativeClassExtension |
Biotin-Responsive Encephalopathy Atypical Inclusion-Body Disease Action Myoclonus-Renal Failure Syndrome Dentatorubral-Pallidoluysian Atrophy Familial Progressive Myoclonic Epilepsy May-White Syndrome |
|
| Resource Identifier |
D020191 |
|
| usageNote |
MeSH includes implied subtypes |
|
| subClassOf |