Concept information
Preferred term
Skin Diseases, Genetic
Type
-
Topical Descriptor
Broader concept
Narrower concepts
- Albinism
- Cutis Laxa
- Darier Disease
- Dermatitis, Atopic
- Dyskeratosis Congenita
- Ectodermal Dysplasia
- Ehlers-Danlos Syndrome
- Epidermolysis Bullosa
- Erythrokeratodermia Variabilis
- Hereditary Autoinflammatory Diseases
- 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
- Muir-Torre Syndrome
- Pemphigus, Benign Familial
- Porokeratosis
- Porphyria, Erythropoietic
- Porphyrias, Hepatic
- Prolidase Deficiency
- Pseudoxanthoma Elasticum
- Rothmund-Thomson Syndrome
- Sjogren-Larsson Syndrome
- Trichothiodystrophy Syndromes
- Xeroderma Pigmentosum
Entry terms
- Disease, Genetic Skin
- Diseases, Genetic Skin
- Genetic Skin Disease
- Genetic Skin Diseases
- Skin Disease, Genetic
Note
- general or unspecified; prefer specifics
Scope note
- Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.
History note
- 98; use explode 1970-97
In other languages
-
Finnish
-
geneettiset ihosairaudet
-
geneettiset ihotaudit
-
genodermatoosit
-
perinnölliset ihosairaudet
-
Swedish
URI
http://www.yso.fi/onto/mesh/D012873
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