CLDN10

PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Unexplained young onset end-stage renal disease
R-numbers: R198
Signed-off version 4.18
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hypokalemic-alkalotic salt-losing tubulopathy, HELIX syndrome, OMIM:617671