Intermediate generalized junctional epidermolysis bullosa
ORPHA:79402Autosomal dominant dystrophic epidermolysis bullosa, Pasini type
ORPHA:216989Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form
ORPHA:79399Autosomal dominant generalized epidermolysis bullosa simplex, severe form
ORPHA:79396Dystrophic epidermolysis bullosa
ORPHA:303Epidermolysis bullosa acquisita
ORPHA:46487Epidermolysis bullosa simplex
ORPHA:304Epidermolysis bullosa simplex due to BP230 deficiency
ORPHA:412181Inherited epidermolysis bullosa
ORPHA:79361Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome
ORPHA:306504Junctional epidermolysis bullosa
ORPHA:305Junctional epidermolysis bullosa inversa
ORPHA:79405Junctional epidermolysis bullosa with pyloric atresia
ORPHA:79403Kindler epidermolysis bullosa
ORPHA:2908Late-onset junctional epidermolysis bullosa
ORPHA:79406Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome
ORPHA:231556Localized epidermolysis bullosa simplex
ORPHA:79400Localized junctional epidermolysis bullosa
ORPHA:251393OBSOLETE: Junctional epidermolysis bullosa, non-Herlitz type
ORPHA:89840Severe generalized junctional epidermolysis bullosa
ORPHA:79404