Mesh term Skin Diseases, Genetic
Browse to parent terms:Genetic Diseases, Inborn
Skin Diseases
Description
Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.Browse to child terms:
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
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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