GRXCR2

glutaredoxin and cysteine rich domain containing 2
OMIM: 615762
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.79
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
?Deafness, autosomal recessive 101, OMIM:615837