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 ×

Cystinosis

Protein defect of cystin transport

ORPHA:213

Congenital intestinal transport defect

ORPHA:104003

Systemic primary carnitine deficiency

CDSP · CUD

ORPHA:158