/acute myeloid leukemia, WT1 gene mutation

acute myeloid leukemia, WT1 gene mutation

Rare Disease

MONDO:0100417

Also Known As

AML, GUD Gene MutationAML, WAGR Gene MutationAML, WIT-2 Gene MutationAML, WT1 gene mutationAML, WT1 mutationAML, WT33 Gene MutationAML, Wilms Tumor 1 Gene MutationAML, Wilms Tumour 1 Gene Mutation

Definition

Any acute myeloid leukemia that has the chromosomal anomaly WT1 gene mutation. (A change in the nucleotide sequence of the WT1 gene.)

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

External Resources

No external resources available.

Related Diseases

childhood acute myeloid leukemia

MONDO:0004996

Rare

acute monocytic leukemia

MONDO:0007896

Rare

acute promyelocytic leukemia

MONDO:0012883

Rare

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

MONDO:0015166

Rare

acute myeloid leukemia by FAB classification

MONDO:0015667

Rare

inherited acute myeloid leukemia

MONDO:0017893

Rare

← Back to All Diseases