Arteritis

Symptom Information:

Symptom ID: HPO:0012089
Synonyms:
Arteritis (disorder) [Orphanet:35690]
Arteritis [Orphanet:35690]
Vascularitis/vasculitides/arteritis [Orphanet:35690]
Arteritis [MedDRA:10003230]
Arteritis NOS [MedDRA:10003230]
Arteritis thrombotic [MedDRA:10003230]
Arteritis, unspecified [MedDRA:10003230]
Endarteritis [MedDRA:10003230]
Inflammatory arterial reaction [MedDRA:10003230]
Inflammatory artery reaction [MedDRA:10003230]
Panarteritis [MedDRA:10003230]
Thromboarteritis [MedDRA:10003230]
Thrombotic arteritis [MedDRA:10003230]
Panarteritis (rare) [OMIM:Panarteritis (rare)]
Quality:
Cross references:
Orphanet:35690 "Vascularitis/vasculitides/arteritis" [Orphanet:35690]
OMIM: "Panarteritis (rare)" [OMIM:Panarteritis (rare)]
UMLS:C0003860 "Arteritis" [Orphanet:35690]
Is a (Direct Parents):
HPO         Abnormality of the systemic arterial tree
Orphanet Vasculitis
Orphanet Abnormality of cardiovascular system physiology
MedDRA Arterial inflammations
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)
             Abnormality of the systemic arterial tree(HPO:0011004)
                Arteritis(HPO:0012089)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular inflammations(MedDRA:10047116)
       Arterial inflammations(MedDRA:10003231)
          Arteritis(HPO:0012089)
Database Frequency: 40 / 7739
Resource:

All diseases associated with this symptom:

Anti-glomerular basement membrane disease (Orphanet:375)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Behçet disease (Orphanet:117)
Blau syndrome (Orphanet:90340)
Buerger disease (Orphanet:36258)
Choreoacanthocytosis (Orphanet:2388)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Cogan syndrome (Orphanet:1467)
Common variable immunodeficiency (Orphanet:1572)
Cryoglobulinemic vasculitis (Orphanet:91138)
Cutaneous leukocytoclastic angiitis (Orphanet:889)
Dermatomyositis (Orphanet:221)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Erythema elevatum diutinum (Orphanet:90000)
Erythromelalgia (Orphanet:1956)
Familial Mediterranean fever (Orphanet:342)
Familial cutaneous collagenoma (Orphanet:53296)
Giant cell arteritis (Orphanet:397)
Granulomatosis with polyangiitis (Orphanet:900)
Hairy cell leukemia variant (Orphanet:300878)
Hughes-Stovin syndrome (Orphanet:228116)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Immunoglobulin A vasculitis (Orphanet:761)
Juvenile dermatomyositis (Orphanet:93672)
Kawasaki disease (Orphanet:2331)
Majeed syndrome (Orphanet:77297)
Malignant atrophic papulosis (Orphanet:679)
Microscopic polyangiitis (Orphanet:727)
Muckle-Wells syndrome (Orphanet:575)
Nail-patella syndrome (Orphanet:2614)
Polyarteritis nodosa (Orphanet:767)
Polymyositis (Orphanet:732)
Relapsing polychondritis (Orphanet:728)
SAPHO syndrome (Orphanet:793)
Schnitzler syndrome (Orphanet:37748)
TRAPS syndrome (Orphanet:32960)
Takayasu arteritis (Orphanet:3287)
Waldenström macroglobulinemia (Orphanet:33226)
Wiskott-Aldrich syndrome (Orphanet:906)