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Level 3: Inherited Epilepsy Syndromes
Level 2: Neurology and neurodevelopmental disorders
Version 5.10
Latest signed off version: v5.0
(1 May 2024)
Component of the following Super Panels:
Paediatric disorders
Unexplained death in infancy and sudden unexplained death in childhood
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review
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
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Sources
- Expert Review Green
- Wessex and West Midlands GLH
- NHS GMS
- Expert
Phenotypes
- {Epilepsy, idiopathic generalized, 10}, OMIM:613060
- {Epilepsy, juvenile myoclonic, susceptibility to}, OMIM:613060
- {Generalized epilepsy with febrile seizures plus, type 5, susceptibility to}, OMIM:613060
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Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.13
Latest signed off version: v6.0
(1 May 2024)
Component of the following Super Panels:
Childhood onset leukodystrophy
Hypotonic infant
Paediatric disorders
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review
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MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
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Sources
- Expert Review Green
- Literature
Phenotypes
- {Epilepsy, idiopathic generalized, 10}, OMIM:613060
- {Epilepsy, juvenile myoclonic, susceptibility to}, OMIM:613060
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