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"

8 matching diseasesClear search ×

Acute promyelocytic leukemia

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

ORPHA:520

Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)

Acute myeloid leukemia · AML

ORPHA:402020

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

Acute myeloid leukemia · AML

ORPHA:402014

Acute myeloid leukemia with t(8;16)(p11;p13) translocation

Acute myeloid leukemia · AML

ORPHA:370026

Acute myeloid leukemia with t(8;21)(q22;q22) translocation

Acute myeloid leukemia · AML

ORPHA:102724

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

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

Acute myeloid leukemia · AML

ORPHA:402023