Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic
Description
Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism. MeSH
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Subtype Terms (32)
Albinism
6 drugs (4 approved, 2 experimental)
Cutis Laxa
1 experimental drug
Darier Disease
1 approved drug
Dermatitis, Atopic
383 drugs (123 approved, 260 experimental)
Dyskeratosis Congenita
12 drugs (11 approved, 1 experimental)
Ehlers-Danlos Syndrome
10 drugs (7 approved, 3 experimental)
Epidermolysis Bullosa
49 drugs (22 approved, 27 experimental)
Erythrokeratodermia Variabilis
Hereditary Autoinflammatory Diseases
4 drugs (3 approved, 1 experimental)
Ichthyosiform Erythroderma, Congenital
1 approved drug
Ichthyosis Vulgaris
2 experimental drugs
Keratoderma, Palmoplantar
1 experimental drug
Leukokeratosis, Hereditary Mucosal
Lipoid Proteinosis of Urbach and Wiethe
Netherton Syndrome
10 drugs (4 approved, 6 experimental)
Pemphigus, Benign Familial
1 approved drug
Porphyrias, Hepatic
1 approved drug
Pseudoxanthoma Elasticum
8 drugs (4 approved, 4 experimental)
Sjogren-Larsson Syndrome
2 experimental drugs
Xeroderma Pigmentosum
3 approved drugs
Phase 3 Indicated Drugs (3)
Phase 2 Indicated Drugs (5)
Organization Involved with Phase 3 Indications (4)
Organization Involved with Phase 2 Indications (3)
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UMLS Data
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