DUX4

double homeobox 4
OMIM: 606009, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red DUX4 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Fascioscapulohumeral muscular dystrophy, MIM#158900
Tags
  • SV/CNV