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14 Result(s)

ORPHA:505652  CDKL5-deficiency disorder

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ORPHA:33069  Dravet syndrome

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ORPHA:1934  Early infantile epileptic encephalopathy

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ORPHA:86911  Epilepsy with myoclonic absences

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ORPHA:163703  Febrile infection-related epilepsy syndrome

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ORPHA:3451  Infantile spasms syndrome

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ORPHA:2382  Lennox-Gastaut syndrome

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ORPHA:293181  Malignant migrating focal seizures of infancy

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ORPHA:308  Progressive myoclonic epilepsy type 1

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ORPHA:778  Rett syndrome

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ORPHA:1444  Ring chromosome 20 syndrome

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ORPHA:544254  SYNGAP1-related developmental and epileptic encephalopathy

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ORPHA:3205  Sturge-Weber syndrome

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ORPHA:805  Tuberous sclerosis complex

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