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Epidermolysis bullosa simplex

rare

Epidermolysis 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.

Identifiers
MONDO:0017610 Orphanet:304
Part of
Inherited epidermolysis bullosa
Also known as
EBS · EEB · epidermolysis bullosa intraepidermic

Subtypes

All diseases Rare only
Disease Subtypes
Suprabasal epidermolysis bullosa simplex 3
Epidermolysis bullosa simplex 1A, generalized severe
Epidermolysis bullosa simplex 1B, generalized intermediate
Epidermolysis bullosa simplex 1C, localized
Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive
Epidermolysis bullosa simplex 2A, generalized severe
Epidermolysis bullosa simplex 2B, generalized intermediate
Epidermolysis bullosa simplex 2C, localized
Epidermolysis bullosa simplex 2E, with migratory circinate erythema
Epidermolysis bullosa simplex 2F, with mottled pigmentation
Epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive
Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency
Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive
Epidermolysis bullosa simplex 5A, Ogna type
Epidermolysis bullosa simplex 5B, with muscular dystrophy
Epidermolysis bullosa simplex 5C, with pyloric atresia
Epidermolysis bullosa simplex 6, generalized, with scarring and hair loss
Epidermolysis bullosa simplex 7, with nephropathy and deafness
Epidermolysis bullosa simplex with anodontia/hypodontia
Epidermolysis bullosa simplex with nail dystrophy

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