Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

7 matching diseasesClear search ×

Polyarteritis nodosa

Küssmaul-Maier disease · PAN

ORPHA:767

Cutaneous polyarteritis nodosa

Cutaneous PAN · Cutaneous periarteritis nodosa

ORPHA:439729

OBSOLETE: Pediatric polyarteritis nodosa

OBSOLETE: PAN, pediatric onset

ORPHA:93564

Primary polyarteritis nodosa

Primary PAN · Primary periarteritis nodosa

ORPHA:439737

Secondary polyarteritis nodosa

Secondary periarteritis nodosa · Secondary PAN

ORPHA:439746

Single-organ polyarteritis nodosa

Single-organ PAN · Single-organ periarteritis nodosa

ORPHA:439755

Systemic polyarteritis nodosa

Systemic PAN · Systemic periarteritis nodosa

ORPHA:439762