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.
An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN.
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
- Anhydrotic Ectodermal Dysplasia, X-Linked
- Anhydrotic Ectodermal Dysplasia, X Linked
- X-Linked Hypohydridic Ectodermal Dysplasia
- X Linked Hypohydridic Ectodermal Dysplasia
- Ectodermal Dysplasia 1, Anhydrotic
- Ectodermal Dysplasia, Hypohydridic, X-Linked
- Anhidrotic Ectodermal Dysplasia, X-Linked
- Anhidrotic Ectodermal Dysplasia, X Linked
- Christ-Siemens-Touraine Syndrome
- Christ Siemens Touraine Syndrome
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 more specific than "Ectodermal Dysplasia 1, Anhidrotic".
This graph shows the total number of publications written about "Ectodermal Dysplasia 1, Anhidrotic" by people in Harvard Catalyst Profiles by year, and whether "Ectodermal Dysplasia 1, Anhidrotic" was a major or minor topic of these publication.
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Below are the most recent publications written about "Ectodermal Dysplasia 1, Anhidrotic" by people in Profiles.
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[Combined Preimplantation Genetic Testing for Aneuploidy and Monogenic Disease in a Mexican Family Affected by X-linked Hypohidrotic Ectodermal Dysplasia]. Rev Invest Clin. 2018; 70(4):164-168.
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A microRNA screen reveals that elevated hepatic ectodysplasin A expression contributes to obesity-induced insulin resistance in skeletal muscle. Nat Med. 2017 Dec; 23(12):1466-1473.
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False-negative sweat chloride testing in a child with cystic fibrosis and undiagnosed hypohidrotic ectodermal dysplasia. Clin Pediatr (Phila). 2014 Oct; 53(12):1203-5.
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Hypohidrotic ectodermal dysplasia, osteopetrosis, lymphedema, and immunodeficiency in an infant with multiple opportunistic infections. Pediatr Dermatol. 2014 Nov-Dec; 31(6):716-21.