Epidermolysis Bullosa Simplex 2d, Generalized, Intermediate or Severe, Autosomal Recessive, is also known as ebs2d. An important gene associated with Epidermolysis Bullosa Simplex 2d, Generalized, Intermediate or Severe, Autosomal Recessive is KRT5 (Keratin 5). Affiliated tissues include skin, and related phenotypes are hearing impairment and global developmental delay