Rare Disease Library

Progressive myoclonic epilepsy

PME · Progressive myoclonus epilepsy

Action myoclonus-renal failure syndrome

AMRF · Progressive myoclonus epilepsy type 4

Lafora disease

EPM2 · PME type 2

Progressive myoclonic epilepsy type 1

Unverricht-Lundborg disease · EPM1

Progressive myoclonic epilepsy type 3

EPM3 · PME type 3

Progressive myoclonic epilepsy type 5

EPM5 · PME type 5

Progressive myoclonic epilepsy type 6

EPM6 · GOSR2-related progressive myoclonus ataxia

Progressive myoclonic epilepsy type 7

EPM7 · MEAK

Progressive myoclonic epilepsy type 8

EPM8 · PME type 8

Progressive myoclonic epilepsy type 9

EPM9 · PME type 9

Progressive myoclonic epilepsy with dystonia

PMED · Progressive myoclonus epilepsy with dystonia

PRDM8-related progressive myoclonus epilepsy

Early-onset Lafora body disease

Dravet syndrome

SMEI · Severe myoclonic epilepsy of infancy

Epilepsy with eyelid myoclonia

EMA · EMEA

Epilepsy with myoclonic-atonic seizures

Doose syndrome · EMAS

Familial adult myoclonic epilepsy

ADCME · Autosomal dominant cortical myoclonus and epilepsy

Familial infantile myoclonic epilepsy

FIME · Familial infantile myoclonus epilepsy

Juvenile myoclonic epilepsy

JME · Juvenile myoclonus epilepsy

Myoclonic epilepsy in non-progressive encephalopathies

Myoclonus epilepsy in non-progressive encephalopathies · Myoclonic status in non-progressive encephalopathies

Myoclonic epilepsy of infancy

Benign myoclonus epilepsy of infancy · Benign myoclonic epilepsy of infancy

Non progressive epilepsy and/or ataxia with myoclonus as a major feature

OBSOLETE: Progressive epilepsy and/or ataxia with myoclonus as a major feature

Progressive myoclonic epilepsy with neuroserpin inclusion bodies

Early onset familial encephalopathy with neuroserpin inclusion bodies

Spinal muscular atrophy-progressive myoclonic epilepsy syndrome

Hereditary myoclonus-progressive distal muscular atrophy syndrome · Jankovic-Rivera syndrome