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"

8 matching diseasesClear search ×

Primary membranoproliferative glomerulonephritis

Mesangiocapillary glomerulonephritis · Primary MPGN

ORPHA:54370

C3 glomerulonephritis

ORPHA:329931

IgA Nephropathy

Berger disease · Berger's disease

ORPHA:ORPHA:93567

Immunotactoid glomerulopathy

Immunotactoid glomerulonephritis

ORPHA:97567

Immunotactoid or fibrillary glomerulopathy

Immunotactoid or fibrillary glomerulonephritis

ORPHA:91137

Non-amyloid fibrillary glomerulopathy

Congo red-negative amyloidosis-like glomerulopathy · Non-amyloid fibrillary glomerulonephritis

ORPHA:97566

Pauci-immune glomerulonephritis

ORPHA:93126

Primary membranous glomerulonephritis

Primary membranous nephropathy · Idiopathic membranous glomerulonephritis

ORPHA:97560