DLX2

distal-less homeobox 2
OMIM: 126255, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red DLX2 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Red DLX2 in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.38
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders
  • review Not set
    Sources
    • Expert
    Red DLX2 in Paediatric pseudo-obstruction syndrome


    Version 1.5
    Latest signed off version: v1.0 (22 Mar 2023)

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Abnormal bowel motility in mice