recessive dystrophic epidermolysis bullosa inversa (MONDO_0019310) (RDEB-I) is rare subtype of dystrophic epidermolysis bullosa (DEB) characterized by blisters and erosions which are primarily confined to intertriginous skin sites, the base of the neck, the uppermost back, and the lumbosacral area. Also known as: RDEB-I, dystrophic epidermolysis bullosa inversa, inverse RDEB, inverse recessive dystrophic epidermolysis bullosa.