polyarteritis nodosa
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 info
- UMLS:C0031036 (Orphanet:767/e)
- Orphanet:767 (MONDO:equivalentTo)
- ICD10CM:M30.0 (Orphanet:767/e)
- MESH:D010488 (Orphanet:767/e)
- SCTID:155441006 (MONDO:equivalentTo)
- GARD:0007360 (MONDO:equivalentTo)
- ICD9:446.0 (MONDO:i2s)
- MedDRA:10036024 (Orphanet:767/e)
- NCIT:C26847 (MONDO:equivalentTo)
- DOID:9810 (MONDO:equivalentTo)
ordo_disease
http://identifiers.org/meddra/10036024
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://purl.obolibrary.org/obo/DOID_9810, http://purl.bioontology.org/ontology/ICD10CM/M30.0, http://identifiers.org/snomedct/155441006, http://identifiers.org/mesh/D010488, http://purl.obolibrary.org/obo/NCIT_C26847, http://purl.obolibrary.org/obo/Orphanet_767, 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
periarteritis, polyarteritis
MONDO:0019170