Genopathy
Gene-Disorder Association · Article
Gene
KMT2A
Lysine Methyltransferase 2A
Disorder
Mixed Phenotype Acute Leukemia With T(9;22)(Q34.1;Q11.2)
First reported 2021
Supporting publications 3
Key publication · disorder Dasatinib-induced chylothorax: An unusual presentation of a common adverse event-A case report with literature review.EJHaem · 2021
Manually curated
Association Review

In brief

The association between KMT2A (Lysine Methyltransferase 2A) and Mixed Phenotype Acute Leukemia With T(9;22)(Q34.1;Q11.2) is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 3
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
KMT2A

The gene

2 source summaries

A gene summary alongside the source descriptions it was distilled from.

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04
Mixed Phenotype Acute Leukemia With T(9;22)(Q34.1;Q11.2)

The disorder

5 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Literature

Reading

3 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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06
Provenance

References & sources

7 references

Every source and publication cited across this dossier, as one numbered reference list.

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