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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:hypersensitivity vasculitis
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Accession:DOID:9809 term browser browse the term
Definition:A hypersensitivity reaction type III disease that is characterized by inflammation and injury to blood vessels and has_symptom purpura, telangiectasia, blistering, urticaria, and ulcers. (DO)
Synonyms:exact_synonym: hypersensitivity vasculitides
 primary_id: RDO:9003516
 xref: GARD:7851;   ICD9CM:446.2;   NCI:C35119
For additional species annotation, visit the Alliance of Genome Resources.


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show annotations for term's descendants           Sort by:
 
allergic cutaneous vasculitis term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Csf3 colony stimulating factor 3 treatment ISO associated with Severe Congenital Neutropenia; RGD PMID:20100783 RGD:11039037 NCBI chrNW_004936490:15,142,526...15,146,375 JBrowse link
Henoch-Schoenlein purpura term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Agt angiotensinogen severity ISO DNA:missense mutation:cds:p.T174M (human)
DNA:missense mutation:cds:p.M235T (human)
RGD PMID:16521052 PMID:20702504 RGD:11039045 RGD:11039055 NCBI chrNW_004936484:19,713,299...19,721,144 JBrowse link
G C3 complement C3 ISO CTD Direct Evidence: marker/mechanism CTD PMID:1353212 NCBI chrNW_004936588:3,985,732...4,023,221 JBrowse link
G Cd86 CD86 molecule treatment ISO protein:increased expression:venous blood, B cell (human) RGD PMID:27030970 RGD:11354986 NCBI chrNW_004936536:8,414,491...8,481,712 JBrowse link
G Hmox1 heme oxygenase 1 ISO protein:increased expression:serum RGD PMID:20013271 RGD:10755701 NCBI chrNW_004936492:5,042,353...5,049,216 JBrowse link
G Igf1 insulin like growth factor 1 ISO protein:increased expression:serum RGD PMID:20013271 RGD:10755701 NCBI chrNW_004936492:11,709,623...11,784,028 JBrowse link
G Il1rn interleukin 1 receptor antagonist ISO DNA:repeats:intron:IVS2+914_1000dup IL1RN*2 (human) RGD PMID:9186886 RGD:6909151 NCBI chrNW_004936783:1,447,158...1,466,331 JBrowse link
G Il27 interleukin 27 ISO mRNA,protein:decreased expression:peripheral blood mononuclear cell, blood serum (human)" RGD PMID:33280050 RGD:126790550 NCBI chrNW_004936501:11,972,715...11,978,152 JBrowse link
G Il5 interleukin 5 ISO protein:increased expression:serum RGD PMID:16787590 RGD:11354946 NCBI chrNW_004936647:2,647,982...2,651,477 JBrowse link
G Kng1 kininogen 1 ISO protein:increased expression:serum RGD PMID:26098644 RGD:11059888 NCBI chrNW_004936578:3,255,335...3,281,296 JBrowse link
G LOC101968921 angiotensin-converting enzyme disease_progression ISO DNA:deletion:intron:IVS16+1464-1751del (human) RGD PMID:15315169 RGD:11038920 NCBI chrNW_004936541:4,157,847...4,178,156 JBrowse link
G Mefv MEFV innate immuity regulator, pyrin susceptibility ISO DNA:mutations:exons:
DNA:mutations:cds:
DNA:mutation:exon:p. E148Q (human)
RGD PMID:20602240 PMID:22451026 PMID:25232290 RGD:11531116 RGD:7349346 RGD:7349347 NCBI chrNW_004936694:970,706...980,605 JBrowse link
G Plat plasminogen activator, tissue type ISO protein:increased expression:plasma (human) RGD PMID:9543574 RGD:11541055 NCBI chrNW_004936785:476,200...503,371 JBrowse link
G Plau plasminogen activator, urokinase ISO CTD Direct Evidence: therapeutic CTD PMID:9002298 PMID:12671112 NCBI chrNW_004936521:5,238,128...5,243,829 JBrowse link
G Pon1 paraoxonase 1 susceptibility ISO DNA:missense mutations:cds:p.L55M, p.Q192R (human) RGD PMID:19967651 RGD:11552576 NCBI chrNW_004936585:4,954,871...4,979,560 JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13774
    disease of anatomical entity 13507
      immune system disease 3868
        hypersensitivity reaction disease 136
          hypersensitivity reaction type III disease 24
            hypersensitivity vasculitis 15
              Henoch-Schoenlein purpura + 14
              allergic cutaneous vasculitis + 1
Path 2
Term Annotations click to browse term
  disease 13774
    disease of anatomical entity 13507
      Immune & Inflammatory Diseases 4381
        immune system disease 3868
          allergic disease 538
            hypersensitivity reaction type III disease 24
              hypersensitivity vasculitis 15
                Henoch-Schoenlein purpura + 14
                allergic cutaneous vasculitis + 1
paths to the root