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 ×

Primary myelofibrosis

Agnogenic myeloid metaplasia · Idiopathic myelofibrosis

ORPHA:824

Acute panmyelosis with myelofibrosis

Acute myelodysplasia with myelofibrosis · Acute myelofibrosis

ORPHA:86843