Vasculitis

Symptom Information:

Symptom ID: HPO:0002633
Synonyms:
Vasculitis (disorder) [Orphanet:35690]
Vasculitis [Orphanet:35690]
Vasculitis [OMIM:Vasculitis]
Vascularitis/vasculitides/arteritis [Orphanet:35690]
Vasculitis [MedDRA:10047115]
Angiitis [MedDRA:10047115]
Digital vasculitis [MedDRA:10047115]
Focal vasculitis [MedDRA:10047115]
Panagiitis [MedDRA:10047115]
Polyangiitis [MedDRA:10047115]
Vasculitis aggravated [MedDRA:10047115]
Vasculitis legs [MedDRA:10047115]
Vasculitis NOS [MedDRA:10047115]
Vasculitis NOS aggravated [MedDRA:10047115]
Vasculitis worsened [MedDRA:10047115]
Quality:
Cross references:
Orphanet:35690 "Vascularitis/vasculitides/arteritis" [Orphanet:35690]
OMIM: "Vasculitis" [OMIM:Vasculitis]
UMLS:C0042384 "Vasculitis" [HPO:0002633]
UMLS:C0042384 "Vasculitis" [Orphanet:35690]
Is a (Direct Parents):
Orphanet Abnormality of cardiovascular system physiology
HPO         Abnormality of the vasculature
MedDRA Vasculitides NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Vasculitis(HPO:0002633)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular inflammations(MedDRA:10047116)
       Vasculitides NEC(MedDRA:10047113)
          Vasculitis(HPO:0002633)
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

AICARDI-GOUTIERES SYNDROME 7 (OMIM:615846)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA (OMIM:603909)
Autoimmune lymphoproliferative syndrome (Orphanet:3261)
COMPLEMENT COMPONENT 4A DEFICIENCY (OMIM:614380)
CREST syndrome (Orphanet:90290)
Familial cutaneous collagenoma (Orphanet:53296)
HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION (OMIM:601979)
Immunodeficiency with factor I anomaly (Orphanet:200418)
Kawasaki disease (Orphanet:2331)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
RHEUMATOID ARTHRITIS (OMIM:180300)