GSX2

GS homeobox 2
OMIM: 616253, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber GSX2 in Intellectual disability


Level 2: Developmental disorders
Version 9.285
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Diencephalic-mesencephalic junction dysplasia syndrome 2 618646
    • Intellectual disability
    • Dystonia
    • Spastic tetra paresis