Ectodermal Dysplasia 1, Anhidrotic

"Ectodermal Dysplasia 1, 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 X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN.

Descriptor ID	D053358
MeSH Number(s)	C16.131.077.350.198 C16.131.831.350.198 C16.320.322.116 C16.320.850.250.198 C17.800.804.350.198 C17.800.827.250.198
Concept/Terms	Ectodermal Dysplasia 1, Anhidrotic Ectodermal Dysplasia 1, Anhidrotic Ectodermal Dysplasia, Hypohydridic, X-Linked Anhidrotic Ectodermal Dysplasia, X-Linked Anhidrotic Ectodermal Dysplasia, X Linked Ectodermal Dysplasia 1, Anhydrotic CST Syndrome CST Syndromes Syndrome, CST Syndromes, CST X-Linked Hypohydridic Ectodermal Dysplasia X Linked Hypohydridic Ectodermal Dysplasia Ectodermal Dysplasia 1 Dysplasia 1, Ectodermal Ectodermal Dysplasia 1s Ectodermal Dysplasia, Anhidrotic, X-Linked Ectodermal Dysplasia, Hypohidrotic, X-Linked Hypohidrotic Ectodermal Dysplasia Christ-Siemens-Touraine Syndrome Christ Siemens Touraine Syndrome Anhydrotic Ectodermal Dysplasia, X-Linked Anhydrotic Ectodermal Dysplasia, X Linked

Below are MeSH descriptors whose meaning is more general than "Ectodermal Dysplasia 1, 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 1, Anhidrotic [C16.131.077.350.198]
Skin Abnormalities [C16.131.831]
Ectodermal Dysplasia [C16.131.831.350]
Ectodermal Dysplasia 1, Anhidrotic [C16.131.831.350.198]
Genetic Diseases, Inborn [C16.320]
Genetic Diseases, X-Linked [C16.320.322]
Ectodermal Dysplasia 1, Anhidrotic [C16.320.322.116]
Skin Diseases, Genetic [C16.320.850]
Ectodermal Dysplasia [C16.320.850.250]
Ectodermal Dysplasia 1, Anhidrotic [C16.320.850.250.198]
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]
Skin Diseases, Genetic [C17.800.827]
Ectodermal Dysplasia [C17.800.827.250]
Ectodermal Dysplasia 1, Anhidrotic [C17.800.827.250.198]

Below are MeSH descriptors whose meaning is related to "Ectodermal Dysplasia 1, Anhidrotic".

Below are MeSH descriptors whose meaning is more specific than "Ectodermal Dysplasia 1, Anhidrotic".

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