Inherited acute myeloid leukemia

rare

An instance of acute myeloid leukemia that is caused by an inherited modification of the individual's genome.

Identifiers: MONDO:0017893 Orphanet:319465
Part of: Acute myeloid leukemia Hereditary disorder of connective tissue
Also known as: familial AML · hereditary acute myeloid leukaemia · hereditary acute myeloid leukemia · inherited AML · Pure familial acute myeloid leukaemia

Subtypes

Disease	ID	Genes
Acute promyelocytic leukemia	MONDO:0012883	RARA
Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)	MONDO:0035639	FLT3
Mixed phenotype acute leukemia with t(v;11q23.3)	MONDO:0035642	FLT3

Rare disease

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