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"

6 matching diseasesClear search ×

Senior-Loken syndrome

Nephronophthisis with retinal dystrophy · Renal dysplasia-retinal aplasia syndrome

ORPHA:3156

Bothnia retinal dystrophy

Västerbotten dystrophy

ORPHA:85128

Juvenile nephronophthisis

ORPHA:93592

Nephronophthisis

ORPHA:655

OBSOLETE: Inherited retinal disorder

OBSOLETE: Retinal dystrophy

ORPHA:71862

Retinal ciliopathy due to mutation in nephronophthisis gene

ORPHA:156180