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"

12 matching diseasesClear search ×

Systemic vasculitis associated with glomerulopathy

ORPHA:567560

Vasculitis

Systemic vasculitis

ORPHA:52759

Secondary interstitial lung disease in childhood and adulthood associated with a systemic vasculitis

Secondary ILD in childhood and adulthood associated with a systemic vasculitis

ORPHA:264973

Secondary interstitial lung disease specific to childhood associated with a systemic vasculitis

Secondary ILD specific to childhood associated with a systemic vasculitis

ORPHA:264709

Cryoglobulinemic vasculitis

Essential cryoglobulinemia · Essential mixed cryoglobulinemia

ORPHA:91138

Hypocomplementemic urticarial vasculitis

Anti-C1q vasculitis · Mac Duffie hypocomplementemic urticarial vasculitis

ORPHA:36412

Immunoglobulin A vasculitis

Anaphylactoid purpura · Henoch-Schönlein purpura

ORPHA:761

Primary angiitis of the central nervous system

Isolated angiitis of the central nervous system · PACNS

ORPHA:140989

Rare pediatric vasculitis

ORPHA:280369

Secondary vasculitis

ORPHA:445197

Systemic polyarteritis nodosa

Systemic PAN · Systemic periarteritis nodosa

ORPHA:439762

Systemic sclerosis

Progressive systemic sclerosis · Scleroderma

ORPHA:90291