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"

7 matching diseasesClear search ×

Familial platelet disorder with associated myeloid malignancy

FPD/AML · FPS/AML

ORPHA:71290

Acute myeloid leukaemia with myelodysplasia-related features

AML with multilineage dysplasia · Acute myeloid leukemia with multilineage dysplasia

ORPHA:86845

Acute myeloid leukemia with minimal differentiation

Acute myeloid leukemia · AML

ORPHA:98832

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

Inherited acute myeloid leukemia

Acute myeloid leukemia · AML

ORPHA:319465

OBSOLETE: Hereditary thrombocytopenia-hematological cancer predisposition syndrome

OBSOLETE: Familial platelet disorder with predisposition to hematological cancer

ORPHA:477697