polyarteritis nodosa
segmental transmural, necrotizing vasculitis
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polyarteritis nodosa
Summary
polyarteritis nodosa is a designated intractable/rare disease[1]. It has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- polyarteritis nodosa's instance of is recorded as designated intractable/rare disease[3].
- polyarteritis nodosa's instance of is recorded as class of disease[4].
- polyarteritis nodosa is a type of vasculitis[5].
- polyarteritis nodosa is a type of disease[6].
- polyarteritis nodosa's Commons category is recorded as Polyarteritis nodosa[7].
- polyarteritis nodosa's symptoms and signs is recorded as inflammation[8].
- polyarteritis nodosa's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/85[9].
- polyarteritis nodosa's ICD-9-CM is recorded as 446.0[10].
- polyarteritis nodosa's NCI Thesaurus ID is recorded as C26847[11].
- polyarteritis nodosa's health specialty is recorded as immunology[12].
- polyarteritis nodosa's health specialty is recorded as rheumatology[13].
- polyarteritis nodosa's exact match is recorded as http://purl.obolibrary.org/obo/DOID_9810[14].
- polyarteritis nodosa's exact match is recorded as http://identifiers.org/doid/DOID:9810[15].
- polyarteritis nodosa's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_767[16].
- polyarteritis nodosa's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
polyarteritis nodosa has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[2] It is known by 12 alternative names across languages and contexts.[18]