FRA10AC1

FRA10A associated CGG repeat 1
OMIM: 608866
PanelMode of inheritanceDetails
1 panel
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
FRA10AC1-related neurodevelopmental disorder