LOXHD1

lipoxygenase homology domains 1
OMIM: 613072
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.39
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Deafness, autosomal recessive 77, OMIM:613079