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Descriptor English: Ectodermal Dysplasia 3, Anhidrotic
Descriptor Spanish: Displasia Ectodérmica Anhidrótica Tipo 3
Descriptor displasia ectodérmica anhidrótica tipo 3
Scope note: Forma autosómica dominante de displasia ectodérmica debida a mutaciones del gen del RECEPTOR EDAR.
Descriptor Portuguese: Displasia Ectodérmica Anidrótica Tipo 3
Descriptor French: Dysplasie ectodermique anhidrotique de type 3
Entry term(s): Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant
Tree number(s): C16.131.077.350.298
C16.131.831.350.298
C16.320.850.250.298
C17.800.804.350.298
C17.800.827.250.298
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D053359
Scope note: An autosomal dominant form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR.
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: Ectodermal Dysplasia (1987-2006)
Public MeSH Note: 2007
History Note: 2007
Related: Edar Receptor MeSH
DeCS ID: 52140
Unique ID: D053359
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2007/01/01
Date of Entry: 2006/07/05
Revision Date: 2015/06/18
Ectodermal Dysplasia 3, Anhidrotic - Preferred
Concept UI M0492747
Scope note An autosomal dominant form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR.
Preferred term Ectodermal Dysplasia 3, Anhidrotic
Entry term(s) Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant



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