GON7

GON7, KEOPS complex subunit
OMIM: 617436
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Galloway-Mowat syndrome 9, OMIM:619603
Component of the following Super Panels:
  • - Unexplained young onset end-stage renal disease
R-numbers: R195
Signed-off version 6.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Galloway-Mowat syndrome MONDO:0009627