"Skin Diseases, Genetic" 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.
Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.
| Descriptor ID |
D012873
|
| MeSH Number(s) |
C16.320.850 C17.800.827
|
| Concept/Terms |
Skin Diseases, Genetic- Skin Diseases, Genetic
- Genetic Skin Diseases
- Disease, Genetic Skin
- Diseases, Genetic Skin
- Genetic Skin Disease
- Skin Disease, Genetic
|
Below are MeSH descriptors whose meaning is more general than "Skin Diseases, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Skin Diseases, Genetic".
- Skin Diseases, Genetic
- Albinism
- Cutis Laxa
- Darier Disease
- Dermatitis, Atopic
- Dyskeratosis Congenita
- Ectodermal Dysplasia
- Ehlers-Danlos Syndrome
- Epidermolysis Bullosa
- Erythrokeratodermia Variabilis
- Hyalinosis, Systemic
- Ichthyosiform Erythroderma, Congenital
- Ichthyosis Bullosa of Siemens
- Ichthyosis Vulgaris
- Ichthyosis, X-Linked
- Incontinentia Pigmenti
- Keratoderma, Palmoplantar
- Leukokeratosis, Hereditary Mucosal
- Lipoid Proteinosis of Urbach and Wiethe
- Monilethrix
- Netherton Syndrome
- Pemphigus, Benign Familial
- Porokeratosis
- Porphyria, Erythropoietic
- Porphyrias, Hepatic
- Prolidase Deficiency
- Pseudoxanthoma Elasticum
- Rothmund-Thomson Syndrome
- Sjogren-Larsson Syndrome
- Trichothiodystrophy Syndromes
- Xeroderma Pigmentosum
This graph shows the total number of publications written about "Skin Diseases, Genetic" by people in this website by year, and whether "Skin Diseases, Genetic" 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 |
|---|
| 2014 | 1 | 0 | 1 |
| 2015 | 2 | 0 | 2 |
| 2018 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Skin Diseases, Genetic" by people in Profiles.
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Dissecting Cellulitis of the Scalp. N Engl J Med. 2023 Apr 27; 388(17):1608.
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Cutaneous manifestations of genodermatoses and primary immunodeficiency. Dermatol Online J. 2019 Jun 15; 25(6).
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Primary Localized Cutaneous Nodular Amyloidosis in the Absence of Systemic Disease. Skinmed. 2019; 17(2):131-133.
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Treatment of Ligneous Conjunctivitis Using Topical Plasminogen Therapy in an 8-Week-Old Female Infant. J Pediatr Ophthalmol Strabismus. 2018 Aug 29; 55:e30-e32.
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Obstetric Management of Loeys-Dietz Syndrome. Obstet Gynecol. 2018 06; 131(6):1080-1084.
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Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families. Int J Dermatol. 2017 Dec; 56(12):1406-1413.
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Actinic Prurigo Cheilitis: A Clinicopathologic Review of 75 Cases. Am J Dermatopathol. 2016 Jun; 38(6):418-22.
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Arterial tortuosity in genetic arteriopathies. Curr Opin Cardiol. 2015 Nov; 30(6):587-93.
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A 7-year-old with indurated skin and unilateral progressive joint immobility: A case of stiff skin syndrome. Dermatol Online J. 2015 Sep 17; 21(9).
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Arterial tortuosity in patients with Filamin A- associated vascular aneurysms. Am J Med Genet A. 2014 Nov; 164A(11):2961-3.