Epidermolysis Bullosa, Junctional D016109

Related MeSH Hierarchy (5)

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

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

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

Description

Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is characterized by generalized blister formation, extensive denudation, and separation and cleavage of the basal cell plasma membranes from the basement membrane.   MeSH

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Phase 2 Indicated Drugs (2)

Phase 1 Indicated Drugs (1)


Organization Involved with Phase 2 Indications (2)

Organization Involved with Phase 1 Indications (1)

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