EIF3B

eukaryotic translation initiation factor 3 subunit B
OMIM: 603917
PanelMode of inheritanceDetails
1 panel
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
EIF3B-related neurodevelopmental disorder with cardiac anomalies and craniofacial dysmorphism