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 ×

Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)

Acute myeloid leukemia · AML

ORPHA:402023

Acute myeloid leukemia with t(9;22)(q34.1;q11.2)

Acute myeloid leukemia · AML

ORPHA:585867

B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1)

B lymphoblastic leukemia lymphoma with t(12;21)(p13;q22); TEL-AML1 · B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1); ETV6-RUNX1

ORPHA:585929