Polyarteritis nodosa (PAN) is a rare, clinically heterogeneous, rheumatologic disease characterized by necrotizing inflammatory lesions affecting small- and medium-sized blood vessels. PAN most commonly affects skin, joints, peripheral nerves, the gut, and the kidney. [ Orphanet:767 ]
Term information
- GARD:0007360 (Orphanet-shared)
- DOID:9810 (MONDO:equivalentTo)
- MESH:D010488 (Orphanet:767)
- ICD9:446.0 (i2s)
- UMLS:C0031036 (Orphanet:767)
- SCTID:155441006 (MONDO:equivalentTo)
- NCIT:C26847 (MONDO:equivalentTo)
- Orphanet:767 (MONDO:equivalentTo)
- MedDRA:10036024 (Orphanet:767)
- COHD:320749 (MONDO:equivalentTo)
- ICD10:M30.0 (Orphanet:767)
ordo_disease
http://identifiers.org/snomedct/155445002
http://identifiers.org/snomedct/286960005
http://identifiers.org/snomedct/66121003
http://identifiers.org/snomedct/195347004
http://identifiers.org/snomedct/266323005
Polyarteritis nodosa (PAN) is a rare, clinically heterogeneous, rheumatologic disease characterized by necrotizing inflammatory lesions affecting small- and medium-sized blood vessels. PAN most commonly affects skin, joints, peripheral nerves, the gut, and the kidney.
http://identifiers.org/meddra/10036024
http://www.orpha.net/ORDO/Orphanet_767
http://purl.obolibrary.org/obo/DOID_9810
http://identifiers.org/snomedct/155441006
http://identifiers.org/mesh/D010488
http://purl.obolibrary.org/obo/NCIT_C26847
http://linkedlifedata.com/resource/umls/id/C0031036
http://purl.obolibrary.org/obo/MONDO_0019724
http://purl.obolibrary.org/obo/MONDO_0016177
Küssmaul-Maier disease
classical polyarteritis nodosa
periarteritis nodosa
panarteritis nodosa
classic polyarteritis nodosa
PAN
polyarteritis nodosa