Vogt–Koyanagi–Harada syndrome
MeSH: D014607ORPHA: 3437
Overview
multisystem disease
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with Vogt–Koyanagi–Harada syndrome, sourced from HPO and Orphanet clinical annotations.
Abnormal eyelash morphologyAbnormal eyebrow morphologyVitiligoHypopigmented skin patchesSparse scalp hairPremature graying of hairPoliosisHeadacheCSF pleocytosisCognitive impairmentTinnitusSensorineural hearing impairmentVisual impairmentCataractRetinal detachmentUveitisBlurred visionIridocyclitisShort staturePosterior subcapsular cataractOcular hypertensionRetinal nerve fiber edemaConjunctival hyperemiaNuchal rigidityChorioretinal hypopigmentationGlaucomaPhotophobiaAlopeciaFeverNauseaVertigoAphasiaEpiphoraPosterior synechiae of the anterior chamberCorneal keratic precipitatesScalp tendernessDalen-Fuchs nodules
Classification & Codes
MeSH Code
D014607Orphanet Code
ORPHA:3437Vogt–Koyanagi–Harada syndrome
| MeSH | D014607 |
| Orphanet | ORPHA:3437 |
| Treatments | 0 drug(s) |
| Symptoms on record | 37 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO