DLX6

distal-less homeobox 6
OMIM: 600030, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red DLX6 in Limb disorders


Version 4.23
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • London South East RGC GSTT
    • Viapath
    Phenotypes
    • Split hand/foot malformation 1
    Tags
    • polygenic
    Red DLX6 in Autism


    Version 0.36

    review Not set
    Sources
    • Expert Review Red
    • SFARI
    Red DLX6 in Skeletal dysplasia

    Level 3: Skeletal dysplasias
    Level 2: Skeletal disorders
    Version 4.65
    Latest signed off version: v4.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Paediatric disorders
  • review Unknown
    Sources
    • NHS GMS
    • Expert Review Red
    Phenotypes
    • Split-hand/foot malformation 1 183600
    • Split-hand/foot malformation 1 with sensorineural hearing loss 220600