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 bulbar paralysis of childhood

Fazio-Londe disease · Progressive bulbar palsy of childhood

ORPHA:56965

Progressive pseudorheumatoid dysplasia

PPD · Progressive pseudorheumatoid arthropathy of childhood

ORPHA:1159

Progressive supranuclear palsy

PSP syndrome

ORPHA:683