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.
| Descriptor ID |
D053358
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| 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
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| 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
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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 this website by year, and whether "Ectodermal Dysplasia 1, Anhidrotic" was a major or minor topic of these publications.
Below are the most recent publications written about "Ectodermal Dysplasia 1, Anhidrotic" by people in Profiles.
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Protocol for the Phase 2 EDELIFE Trial Investigating the Efficacy and Safety of Intra-Amniotic ER004 Administration to Male Subjects with X-Linked Hypohidrotic Ectodermal Dysplasia. Genes (Basel). 2023 01 06; 14(1).
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Lrp6 Dynamic Expression in Tooth Development and Mutations in Oligodontia. J Dent Res. 2021 04; 100(4):415-422.
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Automatic recognition of the XLHED phenotype from facial images. Am J Med Genet A. 2017 Sep; 173(9):2408-2414.
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A novel missense mutation in collagenous domain of EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia. J Genet. 2015 Mar; 94(1):115-9.
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Characterization of X-linked hypohidrotic ectodermal dysplasia (XL-HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging. Am J Med Genet A. 2013 Jul; 161A(7):1585-93.
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Long-term follow-up of implant treatment for oligodontia in an actively growing individual: a clinical report. J Prosthet Dent. 2012 Nov; 108(5):279-85.
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Five-year follow-up treatment of an ectodermal dysplasia patient with maxillary anterior composites and mandibular denture: a clinical report. J Prosthodont. 2010 Jun; 19(4):294-8.
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A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia. J Hum Genet. 2006; 51(12):1133-1137.