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"

3 matching diseasesClear search ×

Progressive retinal dystrophy due to retinol transport defect

Retinol dystrophy-iris coloboma-comedogenic acne syndrome

ORPHA:352718

Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome

ORPHA:488197

Jalili syndrome

Cone rod dystrophy-amelogenesis imperfecta syndrome

ORPHA:1873