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"

10 matching diseasesClear search ×

Primary membranous glomerulonephritis

Primary membranous nephropathy · Idiopathic membranous glomerulonephritis

ORPHA:97560

C3 glomerulonephritis

ORPHA:329931

C3 glomerulopathy

C3 glomerulopathy · C3G

ORPHA:329918

Dense deposit disease

Membranoproliferative glomerulonephritis type 2

ORPHA:93571

Granulomatous mastitis

Idiopathic granulomatous mastitis · IGM

ORPHA:64722

IgA Nephropathy

Berger disease · Berger's disease

ORPHA:ORPHA:93567

Immunoglobulin-mediated membranoproliferative glomerulonephritis

Ig-mediated MPGN · Ig-mediated membranoproliferative glomerulonephritis

ORPHA:329903

Immunotactoid glomerulopathy

Immunotactoid glomerulonephritis

ORPHA:97567

Pauci-immune glomerulonephritis

ORPHA:93126

Primary membranoproliferative glomerulonephritis

Mesangiocapillary glomerulonephritis · Primary MPGN

ORPHA:54370