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"

2 matching diseasesClear search ×

Laryngeal abductor paralysis

Familial vocal cord dysfunction · Gerhardt syndrome

ORPHA:2808

Familial progressive vestibulocochlear dysfunction

ORPHA:1767