"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
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