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<meta name="keywords" content="C1292775, acute myeloid leukaemia with 11q23 (mll) abnormalities, acute myeloid leukaemia with mll abnormalities, acute myeloid leukaemia with t(9;11)(p21.3;q23.3); mllt3-kmt2a, acute myeloid leukaemia with t(9;11)(p22.3;q23.3); mllt3-kmt2a, acute myeloid leukaemia with t(9;11)(p22;q23); mllt3-mll, acute myeloid leukemia with 11q23 (mll) abnormalities, acute myeloid leukemia with 11q23 abnormalities, acute myeloid leukemia with 11q23 abnormality, acute myeloid leukemia with kmt2a rearrangement, acute myeloid leukemia with kmt2a/mll rearrangement, acute myeloid leukemia with mll abnormalities, acute myeloid leukemia with mll rearrangement, acute myeloid leukemia with mllr, acute myeloid leukemia with t(9;11)(p21.3;q23.3); mllt3-kmt2a, acute myeloid leukemia with t(9;11)(p22.3;q23.3); mllt3-kmt2a, acute myeloid leukemia with t(9;11)(p22;q23); mllt3-mll, acute myeloid leukemia, 11q23 abnormalities, acute myeloid leukemia, mll, aml with 11q23 abnormalities, aml with t(9;11)(p22;q23); mllt3-mll, neoplastic process, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="A rare tumor arising from hematopoietic and lymphoid tissues characterized by abnormal proliferation and differentiation of a clonal population of myeloid stem cells carrying unspecific 11q23 abnormalities. Clinical manifestations result from accumulation of malignant myeloid cells within the bone marrow, peripheral blood and other organs, and include leukocytosis, anemia, thrombocytopenia, fatigue, anorexia and weight loss." /><meta name="robots" content="index,nofollow,noarchive" />
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<title>Acute myeloid leukemia with 11q23 abnormalities (Concept Id: C1292775)
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<!--
UID=266234
ConceptID=C1292775
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Acute myeloid leukemia with 11q23 abnormalities</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>266234</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C1292775</a></dd><dt><span class="dotprefix"></span></dt><dd>Neoplastic Process</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
<td>acute myeloid leukaemia with 11q23 (MLL) abnormalities; acute myeloid leukaemia with MLL abnormalities; acute myeloid Leukaemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A; acute myeloid leukaemia with t(9;11)(p22.3;q23.3); MLLT3-KMT2A; acute myeloid leukaemia with t(9;11)(p22;q23); MLLT3-MLL; acute myeloid leukemia with 11q23 (MLL) abnormalities; Acute Myeloid Leukemia with 11q23 Abnormalities; acute myeloid leukemia with 11q23 abnormalities; Acute myeloid leukemia with 11q23 abnormality; Acute Myeloid Leukemia with KMT2A Rearrangement; Acute Myeloid Leukemia with KMT2A/MLL Rearrangement; acute myeloid leukemia with MLL abnormalities; Acute Myeloid Leukemia with MLL Rearrangement; Acute Myeloid Leukemia with MLLr; acute myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A; acute myeloid leukemia with t(9;11)(p22.3;q23.3); MLLT3-KMT2A; acute myeloid leukemia with t(9;11)(p22;q23); MLLT3-MLL; Acute myeloid leukemia, 11q23 abnormalities; Acute myeloid leukemia, MLL; Acute Myeloid Leukemia, MLL; AML with 11q23 abnormalities; AML with t(9;11)(p22;q23); MLLT3-MLL</td></tr>
<tr><td><span class="bold">SNOMED CT: </span></td>
<td>Acute myeloid leukemia, MLL (128829008); Acute myeloid leukemia, 11q23 abnormalities (128829008); Acute myeloid leukemia with 11q23 abnormality (1157157006)</td></tr>
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
<td><a href="https://monarchinitiative.org/disease/MONDO:0020317" target="_blank">MONDO:0020317</a></td></tr>
<tr><td>Orphanet:</td>
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&amp;Expert=98831">ORPHA98831</a></td></tr></tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
<div class="portlet mgSection" id="ID_100">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln">A rare tumor arising from hematopoietic and lymphoid tissues characterized by abnormal proliferation and differentiation of a clonal population of myeloid stem cells carrying unspecific 11q23 abnormalities. Clinical manifestations result from accumulation of malignant myeloid cells within the bone marrow, peripheral blood and other organs, and include leukocytosis, anemia, thrombocytopenia, fatigue, anorexia and weight loss. [from <a title="Orphanet Rare Disease Ontology (ORDO)" href="http://www.orphadata.org/cgi-bin/inc/ordo_orphanet.inc.php" class="defSource" target="_blank">ORDO</a>]</div>
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<div class="portlet mgSection" id="ID_118">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li><li><a href="#tabORDO">Orphanet</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test,  </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test,  </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM,  </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>,  </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar  </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Acute myeloid leukemia with 11q23 abnormalities</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/5483" ref="tree=MeSH" title="MedGen record for Hematologic disorder">Hematologic disorder</a></span><ul><li><span class="TLline"><a href="/medgen/138213" ref="tree=MeSH" title="MedGen record for Hematologic neoplasm">Hematologic neoplasm</a></span><ul><li><span class="TLline"><a href="/medgen/9725" ref="tree=MeSH" title="MedGen record for Leukemia">Leukemia</a></span><ul><li><span class="TLline"><a href="/medgen/43225" ref="tree=MeSH" title="MedGen record for Acute leukemia">Acute leukemia</a></span><ul><li><span class="TLline"><a href="/medgen/9730" ref="tree=MeSH" title="MedGen record for Acute myeloid leukemia">Acute myeloid leukemia</a></span><ul><li><span class="TLline"><a href="/medgen/220899" ref="tree=MeSH" title="MedGen record for Acute myeloid leukemia with recurrent genetic anomaly">Acute myeloid leukemia with recurrent genetic anomaly</a></span><ul><li><span class="matched_ds">Acute myeloid leukemia with 11q23 abnormalities</span><ul><li><span class="TLline"><a href="/medgen/1385022" ref="tree=MeSH" title="MedGen record for Acute Myeloid Leukemia with t(6;11)(q27;q23.3); MLLT4-KMT2A">Acute Myeloid Leukemia with t(6;11)(q27;q23.3); MLLT4-KMT2A</a></span></li><li><span class="TLline"><a href="/medgen/753997" ref="tree=MeSH" title="MedGen record for Acute myeloid leukemia with t(9;11)(p22;q23)">Acute myeloid leukemia with t(9;11)(p22;q23)</a></span><ul><li><span class="TLline"><a href="/medgen/280999" ref="tree=MeSH" title="MedGen record for Adult Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A">Adult Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A</a></span></li><li><span class="TLline"><a href="/medgen/1654885" ref="tree=MeSH" title="MedGen record for Recurrent Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A">Recurrent Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div><div id="tabORDO">Follow <a target="_blank" href="http://www.orpha.net/consor/cgi-bin/Disease_Classif.php?lng=EN&amp;data_id=156&amp;PatId=13848&amp;search=Disease_Classif_Simple&amp;new=1" class="ital bold">this link</a> to review classifications for <span class="ital">Acute myeloid leukemia with 11q23 abnormalities</span> in Orphanet.</div></div></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
<div class="nl"><a target="_blank" href="/pubmed/23349007">Primary myelofibrosis: 2013 update on diagnosis, risk-stratification, and management.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Tefferi A</span><br />
<span class="medgenPMjournal">Am J Hematol</span>
2013 Feb;88(2):141-50.
doi: 10.1002/ajh.23384.
<span class="bold">PMID: </span><a href="/pubmed/23349007" target="_blank">23349007</a></div>
<div class="nl"><a target="_blank" href="/pubmed/22086865">Primary myelofibrosis: 2012 update on diagnosis, risk stratification, and management.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Tefferi A</span><br />
<span class="medgenPMjournal">Am J Hematol</span>
2011 Dec;86(12):1017-26.
doi: 10.1002/ajh.22210.
<span class="bold">PMID: </span><a href="/pubmed/22086865" target="_blank">22086865</a></div>
<div class="nl"><a target="_blank" href="/pubmed/21574543">Genetic abnormalities in leukemia secondary to treatment in patients with Hodgkin's disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Salas C,
Pérez-Vera P,
Frías S</span><br />
<span class="medgenPMjournal">Rev Invest Clin</span>
2011 Jan-Feb;63(1):53-63.
<span class="bold">PMID: </span><a href="/pubmed/21574543" target="_blank">21574543</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(acute%20myeloid%20leukemia%20with%2011q23%20abnormalities)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (18)</a></div></div>
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<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
<div class="nl"><a target="_blank" href="/pubmed/37247302">Cytogenetic Characteristics of de novo Acute Myeloid Leukemia in Southern Vietnam.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Thao LTT,
Ha CT,
Ha NTT,
Beaupha SMC,
Nghia H,
Tung TT,
Son NT,
Binh NT,
Dung PC,
Vu HA,
Xinh PT</span><br />
<span class="medgenPMjournal">Asian Pac J Cancer Prev</span>
2023 May 1;24(5):1789-1795.
doi: 10.31557/APJCP.2023.24.5.1789.
<span class="bold">PMID: </span><a href="/pubmed/37247302" target="_blank">37247302</a><a href="/pmc/articles/PMC10495905" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/36044298">Clinical and Cytogenetic Characteristics of Children With Leukemia 20-Year Retrospective Study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Runjic E,
Jelicic Kadic A,
Bastian L,
Lozic M,
Buljubasic Soda M,
Petrovic M,
Malic Tudor K,
Kuljis D,
Armanda V,
Lozic B</span><br />
<span class="medgenPMjournal">J Pediatr Hematol Oncol</span>
2023 Mar 1;45(2):e161-e166.
Epub 2022 Aug 29
doi: 10.1097/MPH.0000000000002529.
<span class="bold">PMID: </span><a href="/pubmed/36044298" target="_blank">36044298</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34591430">11q23/MLL rearrangements in adult acute leukemia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Zotova OV,
Lukianova AS,
Valchuk MO,
Karol YS,
Shalay OO,
Novak VL,
Loginsky VE</span><br />
<span class="medgenPMjournal">Exp Oncol</span>
2021 Sep;43(3):229-233.
doi: 10.32471/exp-oncology.2312-8852.vol-43-no-3.16495.
<span class="bold">PMID: </span><a href="/pubmed/34591430" target="_blank">34591430</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33020282">Mutational landscape and clinical outcome of patients with de novo acute myeloid leukemia and rearrangements involving 11q23/KMT2A.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Bill M,
Mrózek K,
Kohlschmidt J,
Eisfeld AK,
Walker CJ,
Nicolet D,
Papaioannou D,
Blachly JS,
Orwick S,
Carroll AJ,
Kolitz JE,
Powell BL,
Stone RM,
de la Chapelle A,
Byrd JC,
Bloomfield CD</span><br />
<span class="medgenPMjournal">Proc Natl Acad Sci U S A</span>
2020 Oct 20;117(42):26340-26346.
Epub 2020 Oct 5
doi: 10.1073/pnas.2014732117.
<span class="bold">PMID: </span><a href="/pubmed/33020282" target="_blank">33020282</a><a href="/pmc/articles/PMC7584992" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/20385793">Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Grimwade D,
Hills RK,
Moorman AV,
Walker H,
Chatters S,
Goldstone AH,
Wheatley K,
Harrison CJ,
Burnett AK;
National Cancer Research Institute Adult Leukaemia Working Group</span><br />
<span class="medgenPMjournal">Blood</span>
2010 Jul 22;116(3):354-65.
Epub 2010 Apr 12
doi: 10.1182/blood-2009-11-254441.
<span class="bold">PMID: </span><a href="/pubmed/20385793" target="_blank">20385793</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Acute%20myeloid%20leukemia%20with%2011q23%20abnormalities%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (171)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/37247302">Cytogenetic Characteristics of de novo Acute Myeloid Leukemia in Southern Vietnam.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Thao LTT,
Ha CT,
Ha NTT,
Beaupha SMC,
Nghia H,
Tung TT,
Son NT,
Binh NT,
Dung PC,
Vu HA,
Xinh PT</span><br />
<span class="medgenPMjournal">Asian Pac J Cancer Prev</span>
2023 May 1;24(5):1789-1795.
doi: 10.31557/APJCP.2023.24.5.1789.
<span class="bold">PMID: </span><a href="/pubmed/37247302" target="_blank">37247302</a><a href="/pmc/articles/PMC10495905" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/35038958">MECOM gene overexpression in pediatric patients with acute myeloid leukemia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Elsherif M,
Hammad M,
Hafez H,
Yassin D,
Ashraf M,
Yasser N,
Lehmann L,
Elhaddad A</span><br />
<span class="medgenPMjournal">Acta Oncol</span>
2022 Apr;61(4):516-522.
Epub 2022 Jan 17
doi: 10.1080/0284186X.2022.2025611.
<span class="bold">PMID: </span><a href="/pubmed/35038958" target="_blank">35038958</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34591430">11q23/MLL rearrangements in adult acute leukemia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Zotova OV,
Lukianova AS,
Valchuk MO,
Karol YS,
Shalay OO,
Novak VL,
Loginsky VE</span><br />
<span class="medgenPMjournal">Exp Oncol</span>
2021 Sep;43(3):229-233.
doi: 10.32471/exp-oncology.2312-8852.vol-43-no-3.16495.
<span class="bold">PMID: </span><a href="/pubmed/34591430" target="_blank">34591430</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26071458">Acute Myeloid Leukemia With Recurrent Cytogenetic Abnormalities.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Foucar K,
Anastasi J</span><br />
<span class="medgenPMjournal">Am J Clin Pathol</span>
2015 Jul;144(1):6-18.
doi: 10.1309/AJCPI9C8UILYQTNS.
<span class="bold">PMID: </span><a href="/pubmed/26071458" target="_blank">26071458</a></div>
<div class="nl"><a target="_blank" href="/pubmed/20385793">Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Grimwade D,
Hills RK,
Moorman AV,
Walker H,
Chatters S,
Goldstone AH,
Wheatley K,
Harrison CJ,
Burnett AK;
National Cancer Research Institute Adult Leukaemia Working Group</span><br />
<span class="medgenPMjournal">Blood</span>
2010 Jul 22;116(3):354-65.
Epub 2010 Apr 12
doi: 10.1182/blood-2009-11-254441.
<span class="bold">PMID: </span><a href="/pubmed/20385793" target="_blank">20385793</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Acute%20myeloid%20leukemia%20with%2011q23%20abnormalities%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (188)</a></div><h3 class="subhead">Therapy</h3>
<div class="nl"><a target="_blank" href="/pubmed/21574543">Genetic abnormalities in leukemia secondary to treatment in patients with Hodgkin's disease.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Salas C,
Pérez-Vera P,
Frías S</span><br />
<span class="medgenPMjournal">Rev Invest Clin</span>
2011 Jan-Feb;63(1):53-63.
<span class="bold">PMID: </span><a href="/pubmed/21574543" target="_blank">21574543</a></div>
<div class="nl"><a target="_blank" href="/pubmed/20385793">Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Grimwade D,
Hills RK,
Moorman AV,
Walker H,
Chatters S,
Goldstone AH,
Wheatley K,
Harrison CJ,
Burnett AK;
National Cancer Research Institute Adult Leukaemia Working Group</span><br />
<span class="medgenPMjournal">Blood</span>
2010 Jul 22;116(3):354-65.
Epub 2010 Apr 12
doi: 10.1182/blood-2009-11-254441.
<span class="bold">PMID: </span><a href="/pubmed/20385793" target="_blank">20385793</a></div>
<div class="nl"><a target="_blank" href="/pubmed/12682627">Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Pui CH,
Chessells JM,
Camitta B,
Baruchel A,
Biondi A,
Boyett JM,
Carroll A,
Eden OB,
Evans WE,
Gadner H,
Harbott J,
Harms DO,
Harrison CJ,
Harrison PL,
Heerema N,
Janka-Schaub G,
Kamps W,
Masera G,
Pullen J,
Raimondi SC,
Richards S,
Riehm H,
Sallan S,
Sather H,
Shuster J,
Silverman LB,
Valsecchi MG,
Vilmer E,
Zhou Y,
Gaynon PS,
Schrappe M</span><br />
<span class="medgenPMjournal">Leukemia</span>
2003 Apr;17(4):700-6.
doi: 10.1038/sj.leu.2402883.
<span class="bold">PMID: </span><a href="/pubmed/12682627" target="_blank">12682627</a></div>
<div class="nl"><a target="_blank" href="/pubmed/11919388">Cytogenetic and molecular genetic evolution of chronic myeloid leukemia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Johansson B,
Fioretos T,
Mitelman F</span><br />
<span class="medgenPMjournal">Acta Haematol</span>
2002;107(2):76-94.
doi: 10.1159/000046636.
<span class="bold">PMID: </span><a href="/pubmed/11919388" target="_blank">11919388</a></div>
<div class="nl"><a target="_blank" href="/pubmed/8960104">Molecular diagnosis and monitoring of acute myeloid leukemia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Biondi A,
Rambaldi A</span><br />
<span class="medgenPMjournal">Leuk Res</span>
1996 Oct;20(10):801-7.
doi: 10.1016/s0145-2126(96)00022-7.
<span class="bold">PMID: </span><a href="/pubmed/8960104" target="_blank">8960104</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Acute%20myeloid%20leukemia%20with%2011q23%20abnormalities%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (113)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/38965370">Rearrangements involving 11q23.3/KMT2A in adult AML: mutational landscape and prognostic implications - a HARMONY study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Hernández-Sánchez A,
González T,
Sobas M,
Sträng E,
Castellani G,
Abáigar M,
Valk PJM,
Villaverde Ramiro Á,
Benner A,
Metzeler KH,
Azibeiro R,
Tettero JM,
Martínez-López J,
Pratcorona M,
Martínez Elicegui J,
Mills KI,
Thiede C,
Sanz G,
Döhner K,
Heuser M,
Haferlach T,
Turki AT,
Reinhardt D,
Schulze-Rath R,
Barbus M,
Hernández-Rivas JM,
Huntly B,
Ossenkoppele G,
Döhner H,
Bullinger L</span><br />
<span class="medgenPMjournal">Leukemia</span>
2024 Sep;38(9):1929-1937.
Epub 2024 Jul 4
doi: 10.1038/s41375-024-02333-4.
<span class="bold">PMID: </span><a href="/pubmed/38965370" target="_blank">38965370</a><a href="/pmc/articles/PMC11347382" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/37247302">Cytogenetic Characteristics of de novo Acute Myeloid Leukemia in Southern Vietnam.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Thao LTT,
Ha CT,
Ha NTT,
Beaupha SMC,
Nghia H,
Tung TT,
Son NT,
Binh NT,
Dung PC,
Vu HA,
Xinh PT</span><br />
<span class="medgenPMjournal">Asian Pac J Cancer Prev</span>
2023 May 1;24(5):1789-1795.
doi: 10.31557/APJCP.2023.24.5.1789.
<span class="bold">PMID: </span><a href="/pubmed/37247302" target="_blank">37247302</a><a href="/pmc/articles/PMC10495905" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34591430">11q23/MLL rearrangements in adult acute leukemia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Zotova OV,
Lukianova AS,
Valchuk MO,
Karol YS,
Shalay OO,
Novak VL,
Loginsky VE</span><br />
<span class="medgenPMjournal">Exp Oncol</span>
2021 Sep;43(3):229-233.
doi: 10.32471/exp-oncology.2312-8852.vol-43-no-3.16495.
<span class="bold">PMID: </span><a href="/pubmed/34591430" target="_blank">34591430</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33020282">Mutational landscape and clinical outcome of patients with de novo acute myeloid leukemia and rearrangements involving 11q23/KMT2A.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Bill M,
Mrózek K,
Kohlschmidt J,
Eisfeld AK,
Walker CJ,
Nicolet D,
Papaioannou D,
Blachly JS,
Orwick S,
Carroll AJ,
Kolitz JE,
Powell BL,
Stone RM,
de la Chapelle A,
Byrd JC,
Bloomfield CD</span><br />
<span class="medgenPMjournal">Proc Natl Acad Sci U S A</span>
2020 Oct 20;117(42):26340-26346.
Epub 2020 Oct 5
doi: 10.1073/pnas.2014732117.
<span class="bold">PMID: </span><a href="/pubmed/33020282" target="_blank">33020282</a><a href="/pmc/articles/PMC7584992" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/20385793">Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Grimwade D,
Hills RK,
Moorman AV,
Walker H,
Chatters S,
Goldstone AH,
Wheatley K,
Harrison CJ,
Burnett AK;
National Cancer Research Institute Adult Leukaemia Working Group</span><br />
<span class="medgenPMjournal">Blood</span>
2010 Jul 22;116(3):354-65.
Epub 2010 Apr 12
doi: 10.1182/blood-2009-11-254441.
<span class="bold">PMID: </span><a href="/pubmed/20385793" target="_blank">20385793</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Acute%20myeloid%20leukemia%20with%2011q23%20abnormalities%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (192)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/38225386">Cytogenetic abnormalities predict survival after allogeneic hematopoietic stem cell transplantation for pediatric acute myeloid leukemia: a PDWP/EBMT study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Sharma A,
Galimard JE,
Pryce A,
Bhoopalan SV,
Dalissier A,
Dalle JH,
Locatelli F,
Jubert C,
Mirci-Danicar O,
Kitra-Roussou V,
Bertrand Y,
Fagioli F,
Rialland F,
Biffi A,
Wynn RF,
Michel G,
Tambaro FP,
Al-Ahmari A,
Tbakhi A,
Furness CL,
Diaz MA,
Sedlacek P,
Bodova I,
Faraci M,
Rao K,
Kleinschmidt K,
Petit A,
Gibson B,
Bhatt NS,
Kalwak K,
Corbacioglu S</span><br />
<span class="medgenPMjournal">Bone Marrow Transplant</span>
2024 Apr;59(4):451-458.
Epub 2024 Jan 15
doi: 10.1038/s41409-024-02197-3.
<span class="bold">PMID: </span><a href="/pubmed/38225386" target="_blank">38225386</a></div>
<div class="nl"><a target="_blank" href="/pubmed/35833755">Mutational landscape and clinical outcome of pediatric acute myeloid leukemia with 11q23/KMT2A rearrangements.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Yuen KY,
Liu Y,
Zhou YZ,
Wang Y,
Zhou DH,
Fang JP,
Xu LH</span><br />
<span class="medgenPMjournal">Cancer Med</span>
2023 Jan;12(2):1418-1430.
Epub 2022 Jul 14
doi: 10.1002/cam4.5026.
<span class="bold">PMID: </span><a href="/pubmed/35833755" target="_blank">35833755</a><a href="/pmc/articles/PMC9883550" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/20385793">Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Grimwade D,
Hills RK,
Moorman AV,
Walker H,
Chatters S,
Goldstone AH,
Wheatley K,
Harrison CJ,
Burnett AK;
National Cancer Research Institute Adult Leukaemia Working Group</span><br />
<span class="medgenPMjournal">Blood</span>
2010 Jul 22;116(3):354-65.
Epub 2010 Apr 12
doi: 10.1182/blood-2009-11-254441.
<span class="bold">PMID: </span><a href="/pubmed/20385793" target="_blank">20385793</a></div>
<div class="nl"><a target="_blank" href="/pubmed/15291802">The biological and clinical significance of MLL abnormalities in haematological malignancies.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Mitterbauer-Hohendanner G,
Mannhalter C</span><br />
<span class="medgenPMjournal">Eur J Clin Invest</span>
2004 Aug;34 Suppl 2:12-24.
doi: 10.1111/j.0960-135X.2004.01366.x.
<span class="bold">PMID: </span><a href="/pubmed/15291802" target="_blank">15291802</a></div>
<div class="nl"><a target="_blank" href="/pubmed/10422627">Core-binding factor (CBF) and MLL-associated primary acute myeloid leukemia: biology and clinical implications.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Strout MP,
Marcucci G,
Caligiuri MA,
Bloomfield CD</span><br />
<span class="medgenPMjournal">Ann Hematol</span>
1999 Jun;78(6):251-64.
doi: 10.1007/s002770050511.
<span class="bold">PMID: </span><a href="/pubmed/10422627" target="_blank">10422627</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Acute%20myeloid%20leukemia%20with%2011q23%20abnormalities%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (115)</a></div></div>
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><ul><li><a href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=98831" target="_blank">Orphanet</a></li><li><a href="https://clinicaltrials.gov/search?cond=Acute%20myeloid%20leukemia%20with%2011q23%20abnormalities" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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