| 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 EIF3A-related neurodevelopmental disorder with cardiac anomalies and craniofacial dysmorphism, MONDO:0100038 |