Vogt-Koyanagi-Harada Disease

Alias:
Uveomeningoencephalitic Syndrome
Uveomenigitic Syndrome
Vogt-Koyanagi Syndrome
Harada's Disease
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
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
Related ID:
MESH:D014607
ICD11:1827767178

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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All ages
1-9/100000
29
509
--

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
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