NLM Logo

Ectodermal Dysplasia 3, Anhidrotic MeSH Descriptor Data 2025


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
Ectodermal Dysplasia 3, Anhidrotic Preferred
page delivered in 0.164s