Arteritis
Symptom Information:
Symptom ID: | HPO:0012089 | ||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |