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

Summary

Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2) (MONDO:0035639) is a cancer. A subtype of inherited acute myeloid leukemia — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Classification: Cancer
• Prevalence: Unknown (Worldwide) [Orphanet-validated]

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)
Mondo ID	MONDO:0035639
Orphanet	589534
ICD-10-CM	C92.7
UMLS	C2826037
MedGen	414807
GARD	0022354
Is cancer (heuristic)	yes

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

Data availability: 5 cell lines.

Disease family

This is a subtype of inherited acute myeloid leukemia. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › hematopoietic and lymphoid system neoplasm › hematopoietic and lymphoid cell neoplasm › leukemia › myeloid leukemia › acute myeloid leukemia › inherited acute myeloid leukemia › mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)

Related subtypes (2): acute promyelocytic leukemia, mixed phenotype acute leukemia with t(v;11q23.3)

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.