Ectodermal Dysplasia 3, Anhidrotic

"Ectodermal Dysplasia 3, Anhidrotic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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

Descriptor ID	D053359
MeSH 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
Concept/Terms	Ectodermal Dysplasia 3, Anhidrotic Ectodermal Dysplasia 3, Anhidrotic Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant

Below are MeSH descriptors whose meaning is more general than "Ectodermal Dysplasia 3, Anhidrotic".

Diseases [C]
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 3, Anhidrotic [C16.131.077.350.298]
Skin Abnormalities [C16.131.831]
Ectodermal Dysplasia [C16.131.831.350]
Ectodermal Dysplasia 3, Anhidrotic [C16.131.831.350.298]
Genetic Diseases, Inborn [C16.320]
Skin Diseases, Genetic [C16.320.850]
Ectodermal Dysplasia [C16.320.850.250]
Ectodermal Dysplasia 3, Anhidrotic [C16.320.850.250.298]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Abnormalities [C17.800.804]
Ectodermal Dysplasia [C17.800.804.350]
Ectodermal Dysplasia 3, Anhidrotic [C17.800.804.350.298]
Skin Diseases, Genetic [C17.800.827]
Ectodermal Dysplasia [C17.800.827.250]
Ectodermal Dysplasia 3, Anhidrotic [C17.800.827.250.298]

Below are MeSH descriptors whose meaning is related to "Ectodermal Dysplasia 3, Anhidrotic".

Below are MeSH descriptors whose meaning is more specific than "Ectodermal Dysplasia 3, Anhidrotic".

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