Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

26 matching diseasesClear search ×

Intermediate generalized junctional epidermolysis bullosa

Generalized junctional epidermolysis bullosa, non-Herlitz type · Intermediate generalized JEB

ORPHA:79402

Autosomal dominant generalized dystrophic epidermolysis bullosa

Generalized DDEB

ORPHA:231568

Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form

Epidermolysis bullosa simplex, Koebner type · Epidermolysis bullosa simplex, Köbner type

ORPHA:79399

Autosomal dominant generalized epidermolysis bullosa simplex, severe form

Epidermolysis bullosa simplex, Dowling-Meara type · Autosomal dominant generalized EBS, severe form

ORPHA:79396

Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form

Generalized RDEB, intermediate form · Autosomal recessive dystrophic epidermolysis bullosa generalisata mitis

ORPHA:89842

Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form

Autosomal recessive dystrophic epidermolysis bullosa generalisata gravis · Autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type

ORPHA:79408

Autosomal recessive generalized epidermolysis bullosa simplex

Autosomal recessive generalized EBS

ORPHA:89838

Dystrophic epidermolysis bullosa

DEB · Dermolytic epidermolysis bullosa

ORPHA:303

Dystrophic epidermolysis bullosa pruriginosa

DEB pruriginosa · DEB-Pr

ORPHA:89843

Epidermolysis bullosa acquisita

Acquired epidermolysis bullosa

ORPHA:46487

Epidermolysis bullosa simplex

EBS

ORPHA:304

Epidermolysis bullosa simplex with pyloric atresia

EBS with pyloric atresia · EBS-PA

ORPHA:158684

Inherited epidermolysis bullosa

Epidermolysis bullosa hereditaria · Hereditary epidermolysis bullosa

ORPHA:79361

Junctional epidermolysis bullosa

Epidermolysis bullosa atrophicans · JEB

ORPHA:305

Kindler epidermolysis bullosa

Kindler syndrome · Poikiloderma of Kindler

ORPHA:2908

Late-onset junctional epidermolysis bullosa

JEB-lo · Epidermolysis bullosa progressiva

ORPHA:79406

Localized dystrophic epidermolysis bullosa

Localized DEB

ORPHA:595356

Localized dystrophic epidermolysis bullosa, acral form

Localized DEB, acral form

ORPHA:158673

Localized dystrophic epidermolysis bullosa, nails only

Localized DEB, nails only

ORPHA:158676

Localized dystrophic epidermolysis bullosa, pretibial form

DEB-Pt · Localized DEB, pretibial form

ORPHA:79410

Localized epidermolysis bullosa simplex

EBS-loc · Epidermolysis bullosa simplex of palms and soles

ORPHA:79400

Localized junctional epidermolysis bullosa

JEB-nH loc · Junctional epidermolysis bullosa, non-Herlitz localized type

ORPHA:251393

OBSOLETE: Centripetalis recessive dystrophic epidermolysis bullosa

OBSOLETE: Centripetal dystrophic epidermolysis bullosa · OBSOLETE: Centripetal recessive dystrophic epidermolysis bullosa

ORPHA:89841

Recessive dystrophic epidermolysis bullosa inversa

RDEB inversa · RDEB-I

ORPHA:79409

Self-improving dystrophic epidermolysis bullosa

Self-improving DEB · Transient bullous dermolysis of the newborn

ORPHA:79411

Severe generalized junctional epidermolysis bullosa

Epidermolysis bullosa letalis · JEB-H

ORPHA:79404