FXR1

FMR1 autosomal homolog 1
OMIM: 600819
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Neuromuscular disorders
R-numbers: R81
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Congenital multi-minicore myopathy, ?Myopathy, congenital proximal, with minicore lesions #618823, ?Myopathy, congenital, with respiratory insufficiency and bone fractures #618822