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 ×

Pure autonomic failure

Bradbury-Eggleston syndrome · Idiopathic orthostatic hypotension

ORPHA:441

Lissencephaly due to LIS1 mutation

PAFAH1B1-related lissencephaly

ORPHA:95232