Term Name: junctional epidermolysis bullosa
Synonyms: congenital junctional epidermolysis bullosa
Definition: An epidermolysis bullosa that is characterized by recurrent blistering located in the lamina lucida of the basement membrane secondary to minor trauma, which can cause limited wounds, dehydration, electrolyte abnormalities, severe infection, among other issues, and has_material_basis_in mutation in genes related to laminin 332, which strengthens the skin.
Ontology: Human Disease [DOID:3209]   ( DOID:3209 )

Relationships
is a type of: epidermolysis bullosa
has subtype: junctional epidermolysis bullosa Herlitz type junctional epidermolysis bullosa non-Herlitz type junctional epidermolysis bullosa with pyloric atresia