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"

5 matching diseasesClear search ×

Immunoglobulin A nephropathy

Berger disease · IgA nephropathy

ORPHA:34145

Calpain-3-related limb-girdle muscular dystrophy R1

LGMD2A · Limb-girdle muscular dystrophy due to calpain deficiency

ORPHA:267

IgA Nephropathy

Berger disease · Berger's disease

ORPHA:ORPHA:93567

Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome

Epidermolysis bullosa simplex with nephropathy · Nephrotic syndrome-hearing loss-epidermolysis bullosa syndrome

ORPHA:300333

Primary membranous glomerulonephritis

Primary membranous nephropathy · Idiopathic membranous glomerulonephritis

ORPHA:97560