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"

9 matching diseasesClear search ×

Immunoglobulin-mediated membranoproliferative glomerulonephritis

Ig-mediated MPGN · Ig-mediated membranoproliferative glomerulonephritis

ORPHA:329903

C3 deposition glomerulonephritis without proliferation

ORPHA:93559

C3 glomerulonephritis

ORPHA:329931

C3 glomerulopathy

C3 glomerulopathy · C3G

ORPHA:329918

Dense deposit disease

Membranoproliferative glomerulonephritis type 2

ORPHA:93571

Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome

Hypotrichosis-lymphedema-telangiectasia-membranoproliferative glomerulonephritis syndrome

ORPHA:69735

IgA Nephropathy

Berger disease · Berger's disease

ORPHA:ORPHA:93567

Primary membranoproliferative glomerulonephritis

Mesangiocapillary glomerulonephritis · Primary MPGN

ORPHA:54370

Primary membranous glomerulonephritis

Primary membranous nephropathy · Idiopathic membranous glomerulonephritis

ORPHA:97560