1. Genes and Genomic Entities
  2. DMBX1

DMBX1

diencephalon/mesencephalon homeobox 1
OMIM: 607410, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red DMBX1 in Early onset or syndromic epilepsy

Level 3: Inherited Epilepsy Syndromes
Level 2: Neurology and neurodevelopmental disorders
Version 5.10
Latest signed off version: v5.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Wessex and West Midlands GLH
    • NHS GMS
    • Expert Review Red
    • Literature
    Phenotypes
    • global developmental delay, intellectual disability, and epilepsy