Hair Disease

Hair Disease(来自ICD-11)
别称:
Hair Diseases
Hair Disorder
Hair Problems
Hair Anomaly
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Medical Symptom
Gene & Mutation
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References Literature
Hair Disease, also known as hair disorder, is related to monilethrix and hypotrichosis 7, and has symptoms including exanthema and pruritus. An important gene associated with Hair Disease is KRT86 (Keratin 86), and among its related pathways/superpathways are Keratinization and Innate Lymphoid Cells Differentiation. The drugs Eflornithine and Ornithine have been mentioned in the context of this disorder. Affiliated tissues include skin and cortex, and related phenotypes are homeostasis/metabolism and integument
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相关ID:
MESH:D006201
ICD11:163039429

基础信息

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参考文献
MALACARDS
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Unknown
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56
704
3

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靶点药物

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MGI
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