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"

4 matching diseasesClear search ×

Fragile X-associated primary ovarian insufficiency

FXPOI · Fragile X-associated POI

ORPHA:642691

Rare acquired premature ovarian failure

ORPHA:95709

Rare genetic premature ovarian failure

ORPHA:485382

Rare non-acquired premature ovarian failure

ORPHA:95710