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 ×

Progressive familial intrahepatic cholestasis type 4

TJP2 deficit · PFIC4

ORPHA:480483

Beta-ketothiolase deficiency

3-ketothiolase deficiency · 3-oxothiolase deficiency

ORPHA:134