"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 |
| 2022 | 0 | 1 | 1 |
| 2023 | 1 | 2 | 3 |
| 2024 | 0 | 1 | 1 |
| 2025 | 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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Arterial Tortuosity Syndrome: A Longitudinal Assessment of Cardiovascular Features and Interventions From the Collaborative for Longitudinal Aortic Research in the Young (CLARITY). Am J Med Genet A. 2025 Nov; 197(11):e64159.
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[VEXAS-like auto inflammatory syndrome: 2?cases]. Rev Med Interne. 2025 Mar; 46(3):139-145.
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VEXAS syndrome (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic): clinical review in a rapidly emerging field. Leuk Lymphoma. 2024 Sep; 65(9):1245-1257.
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Vertebral Tortuosity Is Associated With Increased Rate of Cardiovascular Events in Vascular Ehlers-Danlos Syndrome. J Am Heart Assoc. 2023 10 03; 12(19):e029518.
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Dissecting Cellulitis of the Scalp. N Engl J Med. 2023 04 27; 388(17):1608.
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Progressive osseous heteroplasia in a 5-year-old boy with a novel mutation in exon 2 of GNAS: a case presentation and literature review. BMC Musculoskelet Disord. 2023 Mar 31; 24(1):247.
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Aortic tortuosity in Turner syndrome is associated with larger ascending aorta. Int J Cardiovasc Imaging. 2022 Nov; 38(11):2479-2490.
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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.