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Epidermolysis Bullosa, Junctional MeSH Descriptor Data 2023


MeSH Heading
Epidermolysis Bullosa, Junctional
Tree 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
Unique ID
D016109
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D016109
Scope Note
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.
Entry Term(s)
Epidermolysis Bullosa Junctionalis, Disentis Type
Epidermolysis Bullosa Junctionalis, Herlitz Type
Epidermolysis Bullosa Junctionalis, Progressive
Epidermolysis Bullosa Junctionalis, Severe Nonlethal
Epidermolysis Bullosa Letalis
Epidermolysis Bullosa Progressiva
Epidermolysis Bullosa, Generalized Atrophic Benign
Epidermolysis Bullosa, Junctional, Herlitz Type
Epidermolysis Bullosa, Junctional, Herlitz-Pearson Type
Herlitz Disease
Herlitz's Disease
Herlitz-Pearson Type Epidermolysis Bullosa
Herlitz-Pearson-Type Epidermolysis Bullosa
Junctional Epidermolysis Bullosa
Lethal Junctional Epidermolysis Bullosa
Previous Indexing
Epidermolysis Bullosa (1966-1990)
Public MeSH Note
91; HERLITZ DISEASE was HERLITZ'S DISEASE 1991-92
Online Note
use EPIDERMOLYSIS BULLOSA, JUNCTIONAL to search HERLITZ'S DISEASE 1991-92
History Note
91; HERLITZ DISEASE was HERLITZ'S DISEASE 1991-92
Date Established
1991/01/01
Date of Entry
1990/02/12
Revision Date
2015/06/18
Epidermolysis Bullosa, Junctional Preferred
Epidermolysis Bullosa Letalis Narrower
Epidermolysis Bullosa Progressiva Narrower
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