Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
R-numbers: R59 Signed-off version 6.9 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Li-Ghorgani-Weisz-Hubshman syndrome, OMIM:618974, Global developmental delay, Intellectual disability, Seizures, Abnormality of vision, Feeding difficulties, Abnormality of the cardiovascular system, Autism |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 7.51 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Li-Ghorgani-Weisz-Hubshman syndrome, OMIM:618974, Global developmental delay, Intellectual disability, Seizures, Abnormality of vision, Feeding difficulties, Abnormality of the cardiovascular system, Autism |