Skin Disease

Alias:
Skin Diseases
Abnormality of the Skin
Skin Diseases, Genetic
Skin and Subcutaneous Tissue Disease
Type of Genodermatosis
Dermatologic Disorders
Genodermatosis
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Skin Disease, also known as abnormality of the skin, is related to bullous skin disease and peeling skin syndrome, and has symptoms including exanthema, pruritus and enanthema. An important gene associated with Skin Disease is COL17A1 (Collagen Type XVII Alpha 1 Chain), and among its related pathways/superpathways are Phospholipase-C Pathway and Cell junction organization. The drugs Dapsone and Ceftaroline fosamil have been mentioned in the context of this disorder. Affiliated tissues include skin and bone marrow, and related phenotypes are growth/size/body region and hearing/vestibular/ear
Related ID:
MESH:D012871
ICD11:1639304259

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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343
4291
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Medical Symptom

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Description
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Gene & Mutation

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Related Drugs

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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