PanelApp (staging)
  1. Genes and Genomic Entities
  2. DLX6

DLX6

distal-less homeobox 6
OMIM: 600030, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red DLX6 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.302

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

Red DLX6 in Hand and foot malformations


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.76

Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Split-hand/foot malformation 1 183600