DCAF13

DDB1 and CUL4 associated factor 13
OMIM: 616196, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red DCAF13 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neuromuscular disease (MONDO#0019056), DCAF13-related