| 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 9.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes hypomagnesaemia with secondary hypocalcaemia |
Green in Likely inborn error of metabolismComponent of the following Super Panels:
R-numbers: R98 Signed-off version 9.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes hypomagnesaemia with secondary hypocalcaemia |