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C10. Nervous System Diseases: all > Nervous System Diseases [MESH:D009422] > Central Nervous System Diseases [MESH:D002493] > Brain Diseases [MESH:D001927] > Epilepsy [MESH:D004827] > Epilepsies, Myoclonic [MESH:D004831] |
Ataxia with Myoclonic Epilepsy and Presenile Dementia [MESH:C565933] (1)
Deafness, Congenital, and Familial Myoclonic Epilepsy [MESH:C565649] (1)
Epilepsy, Familial Adult Myoclonic, 3 [MESH:C567098] (1)
Epilepsy, Myoclonic, Benign Adult Familial, Type 1 [MESH:C563399] (1)
Epilepsy, Myoclonic, Benign Adult Familial, Type 2 [MESH:C564313] (1)
Familial encephalopathy with neuroserpin inclusion bodies [MESH:C536841] (40)
Feigenbaum Bergeron Richardson syndrome [MESH:C536178] (1)
Hydroxylysinuria [MESH:C565502] (1)
Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders [MESH:C565786] (1)
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