Vogt-Koyanagi-Harada disease
http://purl.obolibrary.org/obo/MONDO_0018092
A bilateral, chronic, diffuse granulomatous panuveitis typically characterized by serous retinal detachment and frequently associated with neurological (meningitis), auditory, and dermatological alterations. [ Orphanet:3437 ]
Term info
- UMLS:C0042170 (Orphanet:3437)
- ICD9:364.24 (MONDO:i2s)
- NCIT:C85218 (MONDO:equivalentTo)
- GARD:0007862 (MONDO:equivalentTo)
- MESH:D014607 (MONDO:equivalentTo)
- DOID:12297 (MONDO:equivalentTo)
- Orphanet:3437 (MONDO:equivalentTo)
- ICD9:363.22 (MONDO:i2s)
- SCTID:193497004 (MONDO:equivalentTo)
gard_rare, ordo_disease
A bilateral, chronic, diffuse granulomatous panuveitis typically characterized by serous retinal detachment and frequently associated with neurological (meningitis), auditory, and dermatological alterations.
http://linkedlifedata.com/resource/umls/id/C0042170, http://identifiers.org/snomedct/193497004, http://purl.obolibrary.org/obo/DOID_12297, http://purl.obolibrary.org/obo/NCIT_C85218, http://purl.obolibrary.org/obo/Orphanet_3437, http://identifiers.org/mesh/D014607
http://purl.obolibrary.org/obo/MONDO_0005071, http://purl.obolibrary.org/obo/MONDO_0002977, http://purl.obolibrary.org/obo/MONDO_0020191, http://purl.obolibrary.org/obo/MONDO_0002254
Vogt-Koyanagi syndrome, uveomeningoencephalitic syndrome, Uveomenigitic syndrome, Harada's disease
VKH disease, VKH syndrome, Vogt-Koyanagi-Harada syndrome
MONDO:0018092
https://rarediseases.info.nih.gov/diseases/7862/vogt-koyanagi-harada-disease