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"

1 matching diseasesClear search ×

Acute promyelocytic leukemia

AML M3 · AML with t(15;17)(q22;q12);(PML/RARalpha) and variants

ORPHA:520