Inherited epidermolysis bullosa
ORPHA:79361OBSOLETE: Hereditary epidermolysis bullosa associated with ocular features
ORPHA:263676Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form
ORPHA:79399Autosomal dominant generalized epidermolysis bullosa simplex, severe form
ORPHA:79396Dystrophic epidermolysis bullosa
ORPHA:303Dystrophic epidermolysis bullosa pruriginosa
ORPHA:89843Epidermolysis bullosa acquisita
ORPHA:46487Epidermolysis bullosa simplex
ORPHA:304Epidermolysis bullosa simplex due to BP230 deficiency
ORPHA:412181Epidermolysis bullosa simplex with anodontia/hypodontia
ORPHA:2325Epidermolysis bullosa simplex with pyloric atresia
ORPHA:158684Intermediate 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 dystrophic epidermolysis bullosa
ORPHA:595356Localized 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:158661Recessive dystrophic epidermolysis bullosa inversa
ORPHA:79409Self-improving dystrophic epidermolysis bullosa
ORPHA:79411Severe generalized junctional epidermolysis bullosa
ORPHA:79404