Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 5.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes MAP4K4-related neurodevelopmental disorder with/without congenital anomalies, multiple congenital anomalies, neurodevelopmental differences |