Genopathy
Gene-Disorder Association · Article
Gene
KMT2A
Lysine Methyltransferase 2A
Manually curatedApproved treatment annotated
Association Review

In brief

The association between KMT2A (Lysine Methyltransferase 2A) and Myelodysplastic Syndrome is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 1
Compounds 1
Trials 116of 410 via KMT2A compounds
Publications 6
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
Myelodysplastic Syndrome

The disorder

11 database identifiers

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

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05
Phenotype

Clinical features

1 clinical feature

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
Interventions

Therapeutics

1 compound or drug

Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.

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07
Human studies

Clinical trials

410 clinical trials

Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.

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08
Literature

Reading

6 publications

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

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09
Provenance

References & sources

12 references

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

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