You are using an outdated browser. Please upgrade your browser to improve your experience.

Vogt-Koyanagi-Harada disease

Disease Summary
Associated Targets (4)
Tchem

2

Tbio

2


Explore Associated Targets
Mondo Description Vogt-Koyanagi-Harada disease is a bilateral, chronic, diffuse granulomatous panuveitis typically characterized by serous retinal detachment and frequently associated with neurological (meningitis), auditory, and dermatological alterations.
Disease Ontology Description An autoimmune hypersensitivity disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis.
Mondo Term and Equivalent IDs
MONDO:0018092:  Vogt-Koyanagi-Harada disease
COHD:4108968: 
GARD:0007862: 
ICD9:363.22: 
ICD9:364.24: 
MESH:D014607: 
NCIT:C85218: 
Orphanet:3437: 
SCTID:193497004: 
UMLS:C0042170: 
GWAS Targets (344)
Target
TDL
Study Count
SNP Count
Beta Count
Odds Ratio
Evidence (Mean Rank Score)
Provenance
Tbio
1
2
0
3
88.3
Tbio
1
2
0
3
88.3
Tbio
1
2
0
3
88.3
Tbio
1
2
0
3
88.3
Tbio
1
2
0
3
88.3
Target
TDL
Beta Count
Odds Ratio
Evidence (Mean Rank Score)
Provenance
Tbio
0
3
88.3
Tbio
0
3
88.3
Tbio
0
3
88.3
Tbio
0
3
88.3
Tbio
0
3
88.3
Target Novelty (Tin-x)