Inherited epidermolysis bullosa
MONDO:0019276Inherited epidermolysis bullosa (EB) encompasses a number of disorders characterized by recurrent blister formation as the result of structural fragility within the skin and selected other tissues.
Also known as: epidermolysis bullosa hereditaria, hereditary epidermolysis bullosa
38 clinical trials for this condition and its sub-types, 5 tagged with Inherited epidermolysis bullosa itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Inherited epidermolysis bullosa
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Epidermolysis bullosa dystrophica 23 trials · 30 incl. sub-types
12 sub-types
- Recessive dystrophic epidermolysis bullosa 21 trials Sub-types →
- Generalized dominant dystrophic epidermolysis bullosa 1 trial
- Acral dystrophic epidermolysis bullosa 0 trials
- Centripetalis recessive dystrophic epidermolysis bullosa 0 trials
- Dystrophic epidermolysis bullosa pruriginosa 0 trials
- Dystrophic epidermolysis bullosa, nails only 0 trials
- Epidermolysis bullosa dystrophica Neurotrophica 0 trials
- Epidermolysis bullosa dystrophica with subcorneal cleavage 0 trials
- Localized dystrophic epidermolysis bullosa 0 trials
- Pretibial dystrophic epidermolysis bullosa 0 trials
- Recessive dystrophic epidermolysis bullosa-generalized other 0 trials
- Transient bullous dermolysis of the newborn 0 trials
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Junctional epidermolysis bullosa 6 trials · 8 incl. sub-types
15 sub-types
- Junctional epidermolysis bullosa, non-Herlitz type 2 trials Sub-types →
- Epidermolysis bullosa, junctional 2A, intermediate 0 trials
- Epidermolysis bullosa, junctional 2B, severe 0 trials
- Epidermolysis bullosa, junctional 3A, intermediate 0 trials
- Epidermolysis bullosa, junctional 3B, severe 0 trials
- Epidermolysis bullosa, junctional 4, intermediate 0 trials
- Epidermolysis bullosa, junctional 5A, intermediate 0 trials
- Epidermolysis bullosa, junctional 6, with pyloric atresia 0 trials
- Epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome 0 trials
- Junctional epidermolysis bullosa Herlitz type 0 trials
- Junctional epidermolysis bullosa inversa 0 trials
- Junctional epidermolysis bullosa with pyloric atresia 0 trials
- Laryngo-onycho-cutaneous syndrome 0 trials
- Late-onset junctional epidermolysis bullosa 0 trials
- Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome 0 trials
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Epidermolysis bullosa simplex 6 trials
20 sub-types
- Epidermolysis bullosa simplex 1B, generalized intermediate 1 trial
- Epidermolysis bullosa simplex 1C, localized 1 trial
- Epidermolysis bullosa simplex 1A, generalized severe 0 trials
- Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive 0 trials
- Epidermolysis bullosa simplex 2A, generalized severe 0 trials
- Epidermolysis bullosa simplex 2B, generalized intermediate 0 trials
- Epidermolysis bullosa simplex 2C, localized 0 trials
- Epidermolysis bullosa simplex 2E, with migratory circinate erythema 0 trials
- Epidermolysis bullosa simplex 2F, with mottled pigmentation 0 trials
- Epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive 0 trials
- Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency 0 trials
- Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive 0 trials
- Epidermolysis bullosa simplex 5A, Ogna type 0 trials
- Epidermolysis bullosa simplex 5B, with muscular dystrophy 0 trials
- Epidermolysis bullosa simplex 5C, with pyloric atresia 0 trials
- Epidermolysis bullosa simplex 6, generalized, with scarring and hair loss 0 trials
- Epidermolysis bullosa simplex 7, with nephropathy and deafness 0 trials
- Epidermolysis bullosa simplex with anodontia/hypodontia 0 trials
- Epidermolysis bullosa simplex with nail dystrophy 0 trials
- Suprabasal epidermolysis bullosa simplex 0 trials Sub-types →
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Kindler syndrome 0 trials
1 sub-type
Most studied deeper sub-types
Epidermolysis bullosa simplex due to plakophilin deficiency
(0)
Epidermolysis bullosa simplex superficialis
(0)
Generalized junctional epidermolysis bullosa non-Herlitz type
(0)
Lethal acantholytic epidermolysis bullosa
(0)
Localized junctional epidermolysis bullosa, non-Herlitz type
(0)
Recessive dystrophic epidermolysis bullosa inversa
(0)