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"

5 matching diseasesClear search ×

B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)

B-ALL with t(9;22)(q34.1;q11.2) · Philadelphia chromosome-like B-ALL

ORPHA:585909

Acute myeloid leukemia with t(6;9)(p23;q34)

Acute myeloid leukemia · AML

ORPHA:402014

Acute myeloid leukemia with t(9;11)(p22;q23)

Acute myeloid leukemia · AML

ORPHA:402017

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

Acute myeloid leukemia · AML

ORPHA:585867

Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)

MPAL with t(9;22)(q34.1;q11.2); BCR-ABL1

ORPHA:589534