JSON

hypocomplementemic urticarial vasculitis

^ http://purl.obolibrary.org/obo/MONDO_0018227

Hypocomplementemic urticarial vasculitis (HUV) is an immune complex-mediated small vessel vasculitis characterized by urticaria and hypocomplementemia (low C1q with or without low C3 and C4), and usually associated with circulating anti-C1q autoantibodies. Arthritis, pulmonary disease, ocular inflammation, and glomerulonephritis are common systemic manifestations. [ Orphanet:36412 ]

Term info

database cross reference
  • SCTID:239945009 (MONDO:equivalentTo)
  • Orphanet:36412 (MONDO:equivalentTo)
  • UMLS:C0343206 (MONDO:equivalentTo)
  • UMLS:CN204757 (MONDO:equivalentTo)
  • GARD:0006725 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

definition

Hypocomplementemic urticarial vasculitis (HUV) is an immune complex-mediated small vessel vasculitis characterized by urticaria and hypocomplementemia (low C1q with or without low C3 and C4), and usually associated with circulating anti-C1q autoantibodies. Arthritis, pulmonary disease, ocular inflammation, and glomerulonephritis are common systemic manifestations.

exactMatch

http://purl.obolibrary.org/obo/Orphanet_36412, http://linkedlifedata.com/resource/umls/id/CN204757, http://linkedlifedata.com/resource/umls/id/C0343206, http://identifiers.org/snomedct/239945009

has exact synonym

anti-C1q vasculitis, McDuffie syndrome, Mac Duffie syndrome, Mac Duffie hypocomplementemic urticarial vasculitis, McDuffie hypocomplementemic urticarial vasculitis

id

MONDO:0018227

seeAlso

https://rarediseases.info.nih.gov/diseases/6725/hypocomplementemic-urticarial-vasculitis