epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive (MONDO_0010976) is a basal subtype of epidermolysis bullosa simplex EBS characterized by generalized or, less frequently, localized acral blistering. Also known as: EBS, autosomal recessive K14, EBS-AR KRT14, KRT14-related autosomal recessive EBS, KRT14-related autosomal recessive epidermolysis bullosa simplex, KRT14-related epidermolysis bullosa simplex, epidermolysis bullosa simplex, autosomal recessive type 1.