| Panel | Mode of inheritance | Details |
|---|---|---|
3 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.3 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes SETD1B associated intellectual disability, epilepsy and autism |
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
R-numbers: R59 Signed-off version 5.10 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Intellectual developmental disorder with seizures and language delay, OMIM:619000, Intellectual developmental disorder with seizures and language delay, MONDO:0033559 |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 6.13 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Intellectual developmental disorder with seizures and language delay, OMIM:619000, Intellectual developmental disorder with seizures and language delay, MONDO:0033559 |