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Disease Myoclonic Epilepsies, Progressive

Name Myoclonic Epilepsies, Progressive
Synonyms Action Myoclonus Renal Failure Syndrome | Action Myoclonus-Renal Failure Syndrome | Ataxia, Chorea, Seizures, And Dementia | Atrophies, Dentatorubral-Pallidoluysian | Atrophy, Dentatorubral-Pallidoluysian | Atypical Inclusion Body Disease | Atypical Inclusion-Body Disease | Atypical Inclusion-Body Diseases | Biotin-Responsive Encephalopathies | Biotin Responsive Encephalopathy | Biotin-Responsive Encephalopathy | Dentatorubral-Pallidoluysian Atrophies | Dentatorubral Pallidoluysian Atrophy | Dentatorubral-Pallidoluysian Atrophy | Disease, Atypical Inclusion-Body | Disease, Naito-Oyanagi | Diseases, Atypical Inclusion-Body | Diseases, Naito-Oyanagi | DRPLA | EEOC | Encephalopathies, Biotin-Responsive | Encephalopathy, Biotin-Responsive | Epilepsies, Progressive Myoclonic | Epilepsies, Progressive Myoclonus | Epilepsy, Progressive Myoclonic | EPILEPSY, PROGRESSIVE MYOCLONIC, 10 | EPILEPSY, PROGRESSIVE MYOCLONIC, 6 | EPILEPSY, PROGRESSIVE MYOCLONIC 7 | EPILEPSY, PROGRESSIVE MYOCLONIC, 8 | EPILEPSY, PROGRESSIVE MYOCLONIC, 9 | Epilepsy, Progressive Myoclonus | EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET | EPM10 | EPM6 | EPM7 | EPM8 | EPM9 | Familial Progressive Myoclonic Epilepsy | Haw River Syndrome | Haw River Syndromes | HRS | Inclusion-Body Disease, Atypical | Inclusion-Body Diseases, Atypical | May White Syndrome | May-White Syndrome | Myoclonic Epilepsy, Progressive | MYOCLONIC EPILEPSY WITH CHOREOATHETOSIS | Myoclonus Epilepsies, Progressive | Myoclonus Nephropathy Syndrome | Myoclonus-Nephropathy Syndrome | Myoclonus-Nephropathy Syndromes | Naito Oyanagi Disease | Naito-Oyanagi Disease | Naito-Oyanagi Diseases | NOD | Oyanagi Disease, Naito | Progressive Myoclonic Epilepsies | Progressive Myoclonic Epilepsy | Progressive Myoclonus Epilepsies | Progressive Myoclonus Epilepsy | River Syndrome, Haw | River Syndromes, Haw | Syndrome, Haw River | Syndrome, Myoclonus-Nephropathy | Syndromes, Haw River | Syndromes, Myoclonus-Nephropathy
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.
Categories Nervous system disease
MeSH® ID D020191
OMIM® IDs 125370 | 614018 | 615369 | 616187 | 616230 | 616540 | 616640
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Top ↑ Ancestors

DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Central Nervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Brain Diseases Has associated chemicals Has associated genes Has associated exposure references Epilepsy Has associated chemicals Has associated genes Epilepsies, Myoclonic Has associated chemicals Has associated genes Myoclonic Epilepsies, Progressive Has associated chemicals Has associated genes

Top ↑ Descendants

Myoclonic Epilepsies, Progressive Has associated chemicals Has associated genes
  Amyotrophic Lateral Sclerosis With Polyglucosan Bodies
  Epilepsy, Progressive Myoclonic 2B
  Epilepsy, Progressive Myoclonic 3
  EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Has associated chemicals Has associated genes
  Lafora Disease Has associated chemicals Has associated genes
  MERRF Syndrome Has associated chemicals Has associated genes
  Myoclonic epilepsy with choreoathetosis
  Prickle1-Related Progressive Myoclonic Epilepsy with Ataxia Has associated chemicals Has associated genes
  SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY Has associated chemicals Has associated genes
  Unverricht-Lundborg Syndrome Has associated chemicals Has associated genes