HMGXB4

HMG-box containing 4
OMIM: 604702, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red HMGXB4 in Intellectual disability


Level 2: Developmental disorders
Version 9.279
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
    • Literature
    Phenotypes
    • Intellectual disability, developmental delay, and dysmorphic features