Search
Descriptor English: Epidermolysis Bullosa Acquisita
Descriptor Spanish: Epidermólisis Ampollosa Adquirida
Descriptor epidermolisis ampollosa adquirida
Entry term(s) epidermolisis bullosa acquisita
epidermolisis bullosa adquirida
Scope note: Forma de epidermolisis bullosa que se caracteriza por la presencia de ampollas subepidérmicas inducidas por traumas, sin historia familiar previa de la enfermedad. La inmunofluorescencia directa muestra depósitos de INMUNOGLOBULINA G en la unión dermo-epidérmica.
Descriptor Portuguese: Epidermólise Bolhosa Adquirida
Descriptor French: Épidermolyse bulleuse acquise
Entry term(s): Acquired Epidermolysis Bullosa
Acquired Form of Epidermolysis Bullosa
Epidermolysis Bullosa, Acquired
Tree number(s): C16.131.831.493.080
C17.800.804.493.080
C17.800.827.275.080
C17.800.865.410.080
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D016107
Scope note: Form of epidermolysis bullosa characterized by trauma-induced, subepidermal blistering with no family history of the disease. Direct immunofluorescence shows IMMUNOGLOBULIN G deposited at the dermo-epidermal junction.
Annotation: note that this is acquired
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Epidermolysis Bullosa (1966-1990)
Public MeSH Note: 91
History Note: 91
DeCS ID: 28924
Unique ID: D016107
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1991/01/01
Date of Entry: 1990/02/12
Revision Date: 2015/06/18
Epidermolysis Bullosa Acquisita - Preferred
Concept UI M0024599
Scope note Form of epidermolysis bullosa characterized by trauma-induced, subepidermal blistering with no family history of the disease. Direct immunofluorescence shows IMMUNOGLOBULIN G deposited at the dermo-epidermal junction.
Preferred term Epidermolysis Bullosa Acquisita
Entry term(s) Acquired Epidermolysis Bullosa
Acquired Form of Epidermolysis Bullosa
Epidermolysis Bullosa, Acquired



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.


Go to survey