Concept information
Término preferido
Skin Diseases, Genetic
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Tipo
-
mesh:Descriptor
Definición
- Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.
Concepto genérico
Conceptos específicos
- 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
Etiquetas alternativas
- Genetic Skin Diseases
En otras lenguas
-
francés
-
Dermatoses génétiques
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Génodermatoses
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Maladies génétiques cutanées
URI
http://data.loterre.fr/ark:/67375/JVR-C32HW0L3-8
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