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Ectodermal Dysplasia 3, Anhidrotic
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Ectodermal Dysplasia 3, Anhidrotic
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
Unique ID
D053359
RDF Unique Identifier
http://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
.
Entry Term(s)
Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant
Previous Indexing
Ectodermal Dysplasia (1987-2006)
See Also
Edar Receptor
Public MeSH Note
2007
History Note
2007
Date Established
2007/01/01
Date of Entry
2006/07/05
Revision Date
2015/06/18
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
Ectodermal Dysplasia [C16.131.077.350]
Ectodermal Dysplasia 1, Anhidrotic [C16.131.077.350.198]
Ectodermal Dysplasia 3, Anhidrotic [C16.131.077.350.298]
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C16.131.077.350.348]
Ellis-Van Creveld Syndrome [C16.131.077.350.398]
Focal Dermal Hypoplasia [C16.131.077.350.424]
Focal Facial Dermal Dysplasias [C16.131.077.350.568]
Neurocutaneous Syndromes [C16.131.077.350.712]
Pachyonychia Congenita [C16.131.077.350.856]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Skin Abnormalities [C16.131.831]
Ectodermal Dysplasia [C16.131.831.350]
Ectodermal Dysplasia 1, Anhidrotic [C16.131.831.350.198]
Ectodermal Dysplasia 3, Anhidrotic [C16.131.831.350.298]
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C16.131.831.350.348]
Ellis-Van Creveld Syndrome [C16.131.831.350.398]
Focal Dermal Hypoplasia [C16.131.831.350.424]
Focal Facial Dermal Dysplasias [C16.131.831.350.568]
Neurocutaneous Syndromes [C16.131.831.350.712]
Pachyonychia Congenita [C16.131.831.350.856]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Skin Diseases, Genetic [C16.320.850]
Ectodermal Dysplasia [C16.320.850.250]
Ectodermal Dysplasia 1, Anhidrotic [C16.320.850.250.198]
Ectodermal Dysplasia 3, Anhidrotic [C16.320.850.250.298]
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C16.320.850.250.348]
Ellis-Van Creveld Syndrome [C16.320.850.250.398]
Focal Dermal Hypoplasia [C16.320.850.250.424]
Focal Facial Dermal Dysplasias [C16.320.850.250.568]
Neurocutaneous Syndromes [C16.320.850.250.712]
Pachyonychia Congenita [C16.320.850.250.856]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Abnormalities [C17.800.804]
Ectodermal Dysplasia [C17.800.804.350]
Ectodermal Dysplasia 1, Anhidrotic [C17.800.804.350.198]
Ectodermal Dysplasia 3, Anhidrotic [C17.800.804.350.298]
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C17.800.804.350.348]
Ellis-Van Creveld Syndrome [C17.800.804.350.398]
Focal Dermal Hypoplasia [C17.800.804.350.424]
Focal Facial Dermal Dysplasias [C17.800.804.350.568]
Neurocutaneous Syndromes [C17.800.804.350.712]
Pachyonychia Congenita [C17.800.804.350.856]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Diseases, Genetic [C17.800.827]
Ectodermal Dysplasia [C17.800.827.250]
Ectodermal Dysplasia 1, Anhidrotic [C17.800.827.250.198]
Ectodermal Dysplasia 3, Anhidrotic [C17.800.827.250.298]
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C17.800.827.250.348]
Ellis-Van Creveld Syndrome [C17.800.827.250.398]
Focal Dermal Hypoplasia [C17.800.827.250.424]
Focal Facial Dermal Dysplasias [C17.800.827.250.568]
Neurocutaneous Syndromes [C17.800.827.250.712]
Pachyonychia Congenita [C17.800.827.250.856]
Expand All
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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
.
Terms
Ectodermal Dysplasia 3, Anhidrotic
Preferred Term
Term UI
T661882
Date
12/09/2005
LexicalTag
NON
ThesaurusID
NLM (2007)
Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant
Term UI
T661883
Date
12/09/2005
LexicalTag
NON
ThesaurusID
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