Genopathy
Gene-Disorder Association · Article
Gene
FLT3
Fms Related Receptor Tyrosine Kinase 3
Disorder
Mixed Phenotype Acute Leukemia With T
First reported 2010
Supporting publications 3
Key publication · disorder PAX-5: a valuable immunohistochemical marker in the differential diagnosis of lymphoid neoplasms.Clinical medicine & research · 2010
Manually curated
Association Review

In brief

The association between FLT3 (Fms Related Receptor Tyrosine Kinase 3) and Mixed Phenotype Acute Leukemia With T is a manually-curated gene–disease association, drawing on a single expert-curated source, which records causative variation.

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
FLT3

The gene

3 source summaries

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

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04
Mixed Phenotype Acute Leukemia With T

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

8 references

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

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