Vogt-Koyanagi-Harada Disease

Vogt-Koyanagi-Harada Disease(来自ICD-11)
别称:
Uveomeningoencephalitic Syndrome
Uveomenigitic Syndrome
Vogt-Koyanagi Syndrome
Harada's Disease
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Basic Information
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References Literature
Vogt-Koyanagi-Harada Disease, also known as uveomeningoencephalitic syndrome, is related to conjunctivitis and uveitis. An important gene associated with Vogt-Koyanagi-Harada Disease is PTPN22 (Protein Tyrosine Phosphatase Non-Receptor Type 22), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Bevacizumab and Growth Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include eye and skin, and related phenotypes are sensorineural hearing impairment and cognitive impairment
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相关ID:
MESH:D014607
ICD11:1827767178

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参考文献
MALACARDS
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All ages
1-9/100000
29
515
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