Epidermolysis bullosa simplex
MONDO:0017610Epidermolysis bullosa simplex (EBS) is a group of hereditary epidermolysis bullosa (HEB) disorders characterized by skin fragility resulting in intraepidermal blisters and erosions that occur either spontaneously or after physical trauma.
Also known as: EBS, EEB, epidermolysis bullosa simplex, epidermolysis bullosa intraepidermic
6 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Epidermolysis bullosa simplex 1B, generalized intermediate
(1)
Epidermolysis bullosa simplex 1A, generalized severe
(0)
Epidermolysis bullosa simplex 1C, localized
(0)
Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive
(0)
Epidermolysis bullosa simplex 2A, generalized severe
(0)
Epidermolysis bullosa simplex 2B, generalized intermediate
(0)
Epidermolysis bullosa simplex 2C, localized
(0)
Epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive
(0)
Epidermolysis bullosa simplex 2E, with migratory circinate erythema
(0)
Epidermolysis bullosa simplex 2F, with mottled pigmentation
(0)
Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
(0)
Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive
(0)
Epidermolysis bullosa simplex 5A, Ogna type
(0)
Epidermolysis bullosa simplex 5B, with muscular dystrophy
(0)
Epidermolysis bullosa simplex 5C, with pyloric atresia
(0)
Epidermolysis bullosa simplex 6, generalized, with scarring and hair loss
(0)
Epidermolysis bullosa simplex 7, with nephropathy and deafness
(0)
Epidermolysis bullosa simplex due to plakophilin deficiency
(0)
Epidermolysis bullosa simplex superficialis
(0)
Epidermolysis bullosa simplex with anodontia/hypodontia
(0)