DLX5

distal-less homeobox 5
OMIM: 600028, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green DLX5 in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Split-hand/foot malformation 1 with sensorineural hearing loss MIM#220600
  • Split-hand/foot malformation 1 MIM#183600

Green DLX5 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.285

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
  • NHS GMS
Phenotypes
  • Split-hand/foot malformation 1 with sensorineural hearing loss 220600

Green DLX5 in Hand and foot malformations


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.74

Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert list
    • Expert Review Green
    • Expert Review Green
    • Expert list
    • NHS GMS
    Phenotypes
    • Split-hand/foot malformation 1 with sensorineural hearing loss 220600

    Green DLX5 in Fetal anomalies


    Version 1.255

    review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Split-hand/foot malformation 1 with sensorineural hearing loss MIM#220600
    • Split-hand/foot malformation 1 MIM#183600