loading...| Preferred Name | vasculitis | |
| Synonyms |
systemic vasculitis |
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| Definitions |
Vasculitis represents a clinically heterogenous group of diseases of multifactorial etiology characterized by inflammation of either large-sized vessels (large-vessel vasculitis, e.g. Giant-cell arteritis and Takayasu arteritis), medium-sized vessels (medium-vessel vasculitis e.g. polyarteritis nodosa and Kawasaki disease), or small-sized vessels (small-vessel vasculitis, e.g. granulomatosis with polyangiitis, microscopic polyangiitis, immunoglobulin A vasculitis, and cutaneous leukocytoclastic angiitis). Vasculitis occurs at any age, may be acute or chronic, and manifests with general symptoms such as fever, weight loss and fatigue, as well as more specific clinical signs depending on the type of vessels and organs affected. The degree of severity is variable, ranging from life or sight threatening disease (e.g. BehC'et disease) to relatively minor skin disease. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0018882 |
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| alternative label |
systemic vasculitis |
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| has narrow synonym |
systemic vasculitis |
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| hasDbXref |
SCTID:31996006 MESH:D014657 Orphanet:52759 GARD:0009565 MedDRA:10047115 UMLS:C0042384 Orphanet:280369 MedDRA:10036023 Wikipedia:Vasculitis NCIT:C26912 EFO:0006803 DOID:865 |
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| imported from | ||
| inSubset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#rare http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders http://purl.oboInOwllibrary.org/oboInOwl/mondo#mondo_rare http://purl.oboInOwllibrary.org/oboInOwl/mondo#disease_grouping http://purl.oboInOwllibrary.org/oboInOwl/mondo#orphanet_rare |
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| label |
vasculitis |
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| prefixIRI |
MONDO:0018882 |
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| prefLabel |
vasculitis |
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| textual definition |
Vasculitis represents a clinically heterogenous group of diseases of multifactorial etiology characterized by inflammation of either large-sized vessels (large-vessel vasculitis, e.g. Giant-cell arteritis and Takayasu arteritis), medium-sized vessels (medium-vessel vasculitis e.g. polyarteritis nodosa and Kawasaki disease), or small-sized vessels (small-vessel vasculitis, e.g. granulomatosis with polyangiitis, microscopic polyangiitis, immunoglobulin A vasculitis, and cutaneous leukocytoclastic angiitis). Vasculitis occurs at any age, may be acute or chronic, and manifests with general symptoms such as fever, weight loss and fatigue, as well as more specific clinical signs depending on the type of vessels and organs affected. The degree of severity is variable, ranging from life or sight threatening disease (e.g. BehC'et disease) to relatively minor skin disease. |
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| subClassOf |