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.

Descriptor ID	D016109
MeSH Number(s)	C16.131.831.493.170 C16.320.850.275.170 C17.800.804.493.170 C17.800.827.275.170 C17.800.865.410.170
Concept/Terms	Epidermolysis Bullosa, Junctional Epidermolysis Bullosa, Junctional Epidermolysis Bullosa, Generalized Atrophic Benign Epidermolysis Bullosa Junctionalis, Severe Nonlethal Junctional Epidermolysis Bullosa Epidermolysis Bullosa Junctionalis, Disentis Type Epidermolysis Bullosa Letalis Epidermolysis Bullosa Letalis Bullosa Letali, Epidermolysis Bullosa Letalis, Epidermolysis Epidermolysis Bullosa Letali Letali, Epidermolysis Bullosa Letalis, Epidermolysis Bullosa Herlitz Disease Disease, Herlitz Lethal Junctional Epidermolysis Bullosa Herlitz-Pearson-Type Epidermolysis Bullosa Bullosa, Herlitz-Pearson-Type Epidermolysis Epidermolysis Bullosa, Herlitz-Pearson-Type Epidermolysis Bullosa, Junctional, Herlitz Type Herlitz-Pearson Type Epidermolysis Bullosa Herlitz Pearson Type Epidermolysis Bullosa Epidermolysis Bullosa Junctionalis, Herlitz Type Herlitz's Disease Disease, Herlitz's Herlitzs Disease Epidermolysis Bullosa, Junctional, Herlitz-Pearson Type Epidermolysis Bullosa Progressiva Epidermolysis Bullosa Progressiva Epidermolysis Bullosa Junctionalis, Progressive

Below are MeSH descriptors whose meaning is more general than "Epidermolysis Bullosa, Junctional".

Below are MeSH descriptors whose meaning is related to "Epidermolysis Bullosa, Junctional".

Below are MeSH descriptors whose meaning is more specific than "Epidermolysis Bullosa, Junctional".