Ectodermal Dysplasia
"Ectodermal Dysplasia" 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.
A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, FOCAL DERMAL HYPOPLASIA, and aplasia cutis congenita.
Descriptor ID |
D004476
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MeSH Number(s) |
C16.131.077.350 C16.131.831.350 C16.320.850.250 C17.800.804.350 C17.800.827.250
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Concept/Terms |
Ectodermal Dysplasia- Ectodermal Dysplasia
- Dysplasia, Ectodermal
- Dysplasias, Ectodermal
- Ectodermal Dysplasias
- Ectodermal Defect, Congenital
- Congenital Ectodermal Defect
- Congenital Ectodermal Defects
- Defects, Congenital Ectodermal
- Ectodermal Defects, Congenital
- Defect, Congenital Ectodermal
Hidrotic Ectodermal Dysplasia- Hidrotic Ectodermal Dysplasia
- Dysplasia, Hidrotic Ectodermal
- Dysplasias, Hidrotic Ectodermal
- Hidrotic Ectodermal Dysplasias
- Hydrotic Ectodermal Dysplasia
- Dysplasia, Hydrotic Ectodermal
- Dysplasias, Hydrotic Ectodermal
- Ectodermal Dysplasia, Hydrotic
- Ectodermal Dysplasias, Hydrotic
- Hydrotic Ectodermal Dysplasias
- Ectodermal Dysplasia, Hidrotic
- Clouston Hidrotic Ectodermal Dysplasia
- Hidrotic Ectodermal Dysplasia, Autosomal Dominant
- Clouston Syndrome
- Syndrome, Clouston
- Ectodermal Dysplasia 2, Hidrotic
- Autosomal Dominant Hidrotic Ectodermal Dysplasia
- Clouston's Hidrotic Ectodermal Dysplasia
- Clouston's Syndrome
- Cloustons Syndrome
- Syndrome, Clouston's
- Ectodermal Dysplasia, Hidrotic, Autosomal Dominant
Anhidrotic Ectodermal Dysplasia- Anhidrotic Ectodermal Dysplasia
- Anhidrotic Ectodermal Dysplasias
- Dysplasia, Anhidrotic Ectodermal
- Dysplasias, Anhidrotic Ectodermal
- Ectodermal Dysplasia, Anhidrotic
- Ectodermal Dysplasias, Anhidrotic
- Ectodermal Dysplasia Anhidrotic
- Anhidrotic, Ectodermal Dysplasia
- Anhidrotics, Ectodermal Dysplasia
- Dysplasia Anhidrotic, Ectodermal
- Dysplasia Anhidrotics, Ectodermal
- Ectodermal Dysplasia, Anhydrotic
- Anhydrotic Ectodermal Dysplasia
- Anhydrotic Ectodermal Dysplasias
- Dysplasia, Anhydrotic Ectodermal
- Dysplasias, Anhydrotic Ectodermal
- Ectodermal Dysplasias, Anhydrotic
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Below are MeSH descriptors whose meaning is more general than "Ectodermal Dysplasia".
Below are MeSH descriptors whose meaning is more specific than "Ectodermal Dysplasia".
This graph shows the total number of publications written about "Ectodermal Dysplasia" by people in this website by year, and whether "Ectodermal Dysplasia" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2015 | 1 | 0 | 1 | 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Ectodermal Dysplasia" by people in Profiles.
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Cadieux-Dion M, Safina NP, Engleman K, Saunders C, Repnikova E, Raje N, Canty K, Farrow E, Miller N, Zellmer L, Thiffault I. Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report. BMC Med Genet. 2018 03 09; 19(1):41.
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Jackson J, Delk P, Farrow E, Griffith C, Lah M, Weaver DD. An infant with large fontanelles, aplasia cutis congenita, tessier facial cleft, polydactyly inversus, and toe syndactyly: a previously undescribed syndrome? Am J Med Genet A. 2015 Apr; 167A(4):683-7.
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