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 ×

Hemifacial spasm

Facial hemispasm · Focal myoclonus of face

ORPHA:221083

Familial cortical myoclonus

ORPHA:319189

Rare myoclonus

ORPHA:306747