| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 7.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes RPS6KC1-related complex neurodevelopmental disorder with spasticity and hypoplasia of corpus callosum, MONDO:0100038 |