CLDND1

claudin domain containing 1
Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red CLDND1 in DDG2P


Version 6.424
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • CLDND1-related leukodystrophy