| Panel | Mode of inheritance | Details |
|---|---|---|
3 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 8.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes AGO1-related developmental disorder (monoallelic) |
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
Signed-off version 9.56 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures, OMIM:620292 |
Green in Intellectual disabilityComponent of the following Super Panels:
Signed-off version 11.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures, OMIM:620292 |