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Vogt-Koyanagi-Harada disease

^ http://www.orpha.net/ORDO/Orphanet_3437


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.

Synonyms: Uveomenigitic syndrome

Term info

database cross reference
  • UMLS:C0042170 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:H30.8 (NTBT (narrower term maps to a broader term))
  • ICD-10:H20.8 (NTBT (narrower term maps to a broader term))
hasDbXref

ICD-10:H20.8, UMLS:C0042170, ICD-10:H30.8

notation

ORPHA:3437