DiseaseID 26749
Vogt-小柳-原田病
Vogt-Koyanagi-Harada Disease
Vogt-Koyanagi-Harada disease is a bilateral, chronic, diffuse granulomatous panuveitis typically characterized by serous retinal detachment and frequently associated with neurological (meningitis), au
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Disease: 1Symptom: 11Target: 12Links: 23
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26749
- Core Entity Id
- 119317
- Source Entity Count
- 1
- Preferred Name
- Vogt-Koyanagi-Harada Disease
- Name Cn
- Vogt-小柳-原田病
- Name Pinyin
- Vogt- Xiao Liu - Yuan Tian Bing
- Name En
- Vogt-Koyanagi-Harada Disease
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- Vogt-Koyanagi-Harada disease is a bilateral, chronic, diffuse granulomatous panuveitis typically characterized by serous retinal detachment and frequently associated with neurological (meningitis), au
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Vogt-Koyanagi-Harada Disease
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Umls
C0042170
Icd10
H20.8H30.8
Sym Map
SMDE04834
Orphanet
3437
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Disease Definition
Vogt-Koyanagi-Harada disease is a bilateral, chronic, diffuse granulomatous panuveitis typically characterized by serous retinal detachment and frequently associated with neurological (meningitis), au