EIF3A

eukaryotic translation initiation factor 3 subunit A
OMIM: 602039
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
EIF3A-related neurodevelopmental disorder with cardiac anomalies and craniofacial dysmorphism, MONDO:0100038