RPH3A

rabphilin 3A
OMIM: 612159, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red RPH3A in DDG2P


Version 8.1
Latest signed off version: v8.0 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • RPH3A-related neurodevelopmental disorder
    Tags
    • de novo