Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
Green in Genetic epilepsy syndromesR-numbers: R59 Signed-off version 3.1 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | 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 |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 4.4 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes {Epilepsy, idiopathic generalized, 10}, OMIM:613060, {Epilepsy, juvenile myoclonic, susceptibility to}, OMIM:613060 |