1. Genes and Genomic Entities
  2. DHX32

DHX32

DEAH-box helicase 32 (putative)
OMIM: 607960, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber DHX32 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 MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Intellectual disability, spastic diplegia, dystonia, brain abnormalities