Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form
ORPHA:79399Autosomal dominant generalized epidermolysis bullosa simplex, severe form
ORPHA:79396Autosomal recessive generalized epidermolysis bullosa simplex
ORPHA:89838Dystrophic epidermolysis bullosa
ORPHA:303Epidermolysis bullosa acquisita
ORPHA:46487Epidermolysis bullosa simplex
ORPHA:304Epidermolysis bullosa simplex due to BP230 deficiency
ORPHA:412181Epidermolysis bullosa simplex due to exophilin 5 deficiency
ORPHA:412189Epidermolysis bullosa simplex with anodontia/hypodontia
ORPHA:2325Epidermolysis bullosa simplex with circinate migratory erythema
ORPHA:158681Epidermolysis bullosa simplex with extracutaneous involvement
ORPHA:595351Epidermolysis bullosa simplex with mottled pigmentation
ORPHA:79397Epidermolysis bullosa simplex with muscular dystrophy
ORPHA:257Epidermolysis bullosa simplex with pyloric atresia
ORPHA:158684Epidermolysis bullosa simplex without extracutaneous involvement
ORPHA:595346Inherited epidermolysis bullosa
ORPHA:79361Intermediate epidermolysis bullosa simplex with cardiomyopathy
ORPHA:508529Intermediate generalized junctional epidermolysis bullosa
ORPHA:79402Junctional epidermolysis bullosa
ORPHA:305Junctional epidermolysis bullosa inversa
ORPHA:79405Kindler epidermolysis bullosa
ORPHA:2908Late-onset junctional epidermolysis bullosa
ORPHA:79406Localized epidermolysis bullosa simplex
ORPHA:79400Localized junctional epidermolysis bullosa
ORPHA:251393Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome
ORPHA:300333OBSOLETE: Basal epidermolysis bullosa simplex
ORPHA:158665OBSOLETE: Epidermolysis bullosa simplex superficialis
ORPHA:89839OBSOLETE: Junctional epidermolysis bullosa, non-Herlitz type
ORPHA:89840OBSOLETE: Suprabasal epidermolysis bullosa simplex
ORPHA:158661Self-improving dystrophic epidermolysis bullosa
ORPHA:79411Severe generalized junctional epidermolysis bullosa
ORPHA:79404