Ectodermal Dysplasia 3, Anhidrotic

An autosomal dominant form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR.

Year introduced: 2007

PubMed search builder options

Subheadings:

Restrict to MeSH Major Topic.

Do not include MeSH terms found below this term in the MeSH hierarchy.

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

MeSH Unique ID: D053359

Entry Terms:

• Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant

Previous Indexing:

• Ectodermal Dysplasia (1987-2006)

See Also:

• Edar Receptor

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Ectodermal Dysplasia
Ectodermal Dysplasia 3, Anhidrotic

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Skin Abnormalities
Ectodermal Dysplasia
Ectodermal Dysplasia 3, Anhidrotic

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Ectodermal Dysplasia
Ectodermal Dysplasia 3, Anhidrotic

All MeSH Categories
Diseases Category
Skin and Connective Tissue Diseases
Skin Diseases
Skin Abnormalities
Ectodermal Dysplasia
Ectodermal Dysplasia 3, Anhidrotic

All MeSH Categories
Diseases Category
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Genetic
Ectodermal Dysplasia
Ectodermal Dysplasia 3, Anhidrotic