MeSH Browser

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: 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.
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)

Ectodermal Dysplasia 3, Anhidrotic MeSH Descriptor Data 2025