| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 7.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes RYBP-related neurodevelopmental disorder with congenital anomalies, complex neurodevelopmental disorder, MONDO:0100038 |