Epidermolysis Bullosa Simplex D016110

Related MeSH Hierarchy (5)

Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Abnormalities » Epidermolysis Bullosa » Epidermolysis Bullosa Simplex

Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Epidermolysis Bullosa » Epidermolysis Bullosa Simplex

Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Vesiculobullous » Epidermolysis Bullosa » Epidermolysis Bullosa Simplex

Description

A form of epidermolysis bullosa characterized by serous bullae that heal without scarring. Mutations in the genes that encode KERATIN-5 and KERATIN-14 have been associated with several subtypes of epidermolysis bullosa simplex.   MeSH

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Phase 1 Indicated Drugs (2)


Organization Involved with Phase 3 Indications (2)

Organization Involved with Phase 1 Indications (1)

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