Panel | Mode of inheritance | Details |
---|---|---|
4 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 3.79 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes FAMILIAL FOCAL EPILEPSY WITH VARIABLE FOCI 604364 |
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
R-numbers: R59 Signed-off version 4.134 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Epilepsy, familial focal, with variable foci 1, OMIM:604364 |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 5.343 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Epilepsy, familial focal, with variable foci 1, OMIM:604364 |
Component of the following Super Panels:
Signed-off version 4.12 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Epilepsy, familial focal, with variable foci 1, OMIM:604364, Focal cortical dysplasia |