CLDN10

claudin 10
OMIM: 617579, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green CLDN10 in Renal tubulopathies


Level 2: Renal
Version 5.11
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Unexplained young onset end-stage renal disease
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Hypokalemic-alkalotic salt-losing tubulopathy
    • HELIX syndrome, OMIM:617671