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Entry
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- #140000 - HAND-FOOT-GENITAL SYNDROME; HFG
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- OMIM
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<p>
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<span class="h4">#140000</span>
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<br />
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<strong>Table of Contents</strong>
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<a href="#title"><strong>Title</strong></a>
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<a href="#phenotypeMap"><strong>Phenotype-Gene Relationships</strong></a>
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<li role="presentation">
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<a href="/clinicalSynopsis/140000"><strong>Clinical Synopsis</strong></a>
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<a href="#text"><strong>Text</strong></a>
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<a href="#description">Description</a>
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<a href="#clinicalFeatures">Clinical Features</a>
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<a href="#inheritance">Inheritance</a>
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<a href="#molecularGenetics">Molecular Genetics</a>
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<a href="#references"><strong>References</strong></a>
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<a href="#contributors"><strong>Contributors</strong></a>
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<li role="presentation">
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<a href="#creationDate"><strong>Creation Date</strong></a>
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<li role="presentation">
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<a href="#editHistory"><strong>Edit History</strong></a>
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<div style="display: table-cell;">External Links</div>
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</a>
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</h4>
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</div>
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<span class="small">
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<a href="#mimClinicalResourcesLinksFold" id="mimClinicalResourcesLinksToggle" class=" mimSingletonTriangleToggle" role="button" data-toggle="collapse" data-parent="#mimExternalLinksAccordion">
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<div style="display: table-row">
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<div id="mimClinicalResourcesLinksToggleTriangle" class="small mimSingletonTriangle" style="color: #337CB5; display: table-cell;">▼</div>
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<div style="display: table-cell;">Clinical Resources</div>
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</div>
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</a>
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</span>
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</span>
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<div id="mimClinicalResourcesLinksFold" class="panel-collapse collapse in mimLinksFold" role="tabpanel" aria-labelledby="clinicalResources">
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<div class="panel-body small mim-panel-body">
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<div><a href="https://clinicaltrials.gov/search?cond=HAND-FOOT-GENITAL SYNDROME" class="mim-tip-hint" title="A registry of federally and privately supported clinical trials conducted in the United States and around the world." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Clinical Trials', 'domain': 'clinicaltrials.gov'})">Clinical Trials</a></div>
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<div><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=2259&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></div>
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<div><a href="https://www.ncbi.nlm.nih.gov/books/NBK1423/" class="mim-tip-hint" title="Expert-authored, peer-reviewed descriptions of inherited disorders including the uses of genetic testing in diagnosis, management, and genetic counseling." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Gene Reviews', 'domain': 'ncbi.nlm.nih.gov'})">Gene Reviews</a></div>
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<div><a href="https://www.diseaseinfosearch.org/x/3232" class="mim-tip-hint" title="Network of disease-specific advocacy organizations, universities, private companies, government agencies, and public policy organizations." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Genetic Alliance', 'domain': 'diseaseinfosearch.org'})">Genetic Alliance</a></div>
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<div><a href="https://medlineplus.gov/genetics/condition/hand-foot-genital-syndrome" class="mim-tip-hint" title="Consumer-friendly information about the effects of genetic variation on human health." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MedlinePlus Genetics', 'domain': 'medlineplus.gov'})">MedlinePlus Genetics</a></div>
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<div><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=140000[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></div>
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<div><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=2438" class="mim-tip-hint" title="European reference portal for information on rare diseases and orphan drugs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">OrphaNet</a></div>
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<div><a href="https://www.possumcore.com/nuxeo/nxdoc/default/07a15097-3150-4d67-9ac2-6b4684c430a8/view_documents?source=omim" class="mim-tip-hint" title="A dysmorphology database of multiple malformations; metabolic, teratogenic, chromosomal, and skeletal syndromes; and their images." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'POSSUM', 'domain': 'possum.net.au'})">POSSUM</a></div>
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<div class="panel-heading mim-panel-heading" role="tab" id="mimAnimalModels">
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<span class="panel-title">
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<span class="small">
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<a href="#mimAnimalModelsLinksFold" id="mimAnimalModelsLinksToggle" class="collapsed mimSingletonTriangleToggle" role="button" data-toggle="collapse" data-parent="#mimExternalLinksAccordion">
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<div style="display: table-row">
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<div id="mimAnimalModelsLinksToggleTriangle" class="small mimSingletonTriangle" style="color: #337CB5; display: table-cell;">►</div>
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<div style="display: table-cell;">Animal Models</div>
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</div>
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</a>
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</span>
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</span>
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</div>
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<div id="mimAnimalModelsLinksFold" class="panel-collapse collapse mimLinksFold" role="tabpanel">
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<div class="panel-body small mim-panel-body">
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<div><a href="https://www.alliancegenome.org/disease/DOID:0060739" class="mim-tip-hint" title="Search Across Species; explore model organism and human comparative genomics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Alliance Genome', 'domain': 'alliancegenome.org'})">Alliance Genome</a></div>
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<div><a href="http://www.informatics.jax.org/disease/140000" class="mim-tip-hint" title="Phenotypes, alleles, and disease models from Mouse Genome Informatics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MGI Mouse Phenotype', 'domain': 'informatics.jax.org'})">MGI Mouse Phenotype</a></div>
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<span>
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<span class="mim-tip-bottom" qtip_title="<strong>Looking for this gene or this phenotype in other resources?</strong>" qtip_text="Select a related resource from the dropdown menu and click for a targeted link to information directly relevant.">
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<div class="col-lg-8 col-lg-pull-2 col-md-8 col-md-pull-2 col-sm-8 col-sm-pull-2 col-xs-12">
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<a id="title" class="mim-anchor"></a>
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<div>
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<a id="number" class="mim-anchor"></a>
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<div class="text-right">
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<a href="#" class="mim-tip-icd" qtip_title="<strong>ICD+</strong>" qtip_text="
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<strong>SNOMEDCT:</strong> 702425002<br />
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<strong>ORPHA:</strong> 2438<br />
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<strong>DO:</strong> 0060739<br />
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">ICD+</a>
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<div>
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<span class="h3">
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<span class="mim-font mim-tip-hint" title="Phenotype description, molecular basis known">
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<span class="text-danger"><strong>#</strong></span>
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140000
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</span>
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</span>
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</div>
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</div>
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<div>
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<a id="preferredTitle" class="mim-anchor"></a>
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<h3>
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<span class="mim-font">
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HAND-FOOT-GENITAL SYNDROME; HFG
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</span>
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</h3>
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</div>
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<div>
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<br />
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</div>
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<div>
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<a id="alternativeTitles" class="mim-anchor"></a>
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<div>
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<p>
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<span class="mim-font">
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<em>Alternative titles; symbols</em>
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</span>
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</p>
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</div>
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<div>
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<h4>
|
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<span class="mim-font">
|
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HAND-FOOT-UTERUS SYNDROME; HFU
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</span>
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</h4>
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</div>
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</div>
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<div>
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<br />
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</div>
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</div>
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<div>
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<a id="phenotypeMap" class="mim-anchor"></a>
|
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<h4>
|
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<span class="mim-font">
|
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<strong>Phenotype-Gene Relationships</strong>
|
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</span>
|
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</h4>
|
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<div>
|
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<table class="table table-bordered table-condensed table-hover small mim-table-padding">
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<thead>
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<tr class="active">
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<th>
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Location
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</th>
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<th>
|
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Phenotype
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</th>
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<th>
|
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Phenotype <br /> MIM number
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</th>
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<th>
|
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Inheritance
|
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</th>
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<th>
|
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Phenotype <br /> mapping key
|
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</th>
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<th>
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Gene/Locus
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</th>
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<th>
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Gene/Locus <br /> MIM number
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</th>
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</thead>
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<tbody>
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<tr>
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<td>
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<span class="mim-font">
|
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<a href="/geneMap/7/145?start=-3&limit=10&highlight=145">
|
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7p15.2
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</a>
|
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</span>
|
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</td>
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<td>
|
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<span class="mim-font">
|
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Hand-foot-genital syndrome
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</span>
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</td>
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<td>
|
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<span class="mim-font">
|
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<a href="/entry/140000"> 140000 </a>
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</span>
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</td>
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<td>
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<span class="mim-font">
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<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
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</td>
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<td>
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<span class="mim-font">
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<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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</td>
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<td>
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<span class="mim-font">
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HOXA13
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</span>
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</td>
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<td>
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<span class="mim-font">
|
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<a href="/entry/142959"> 142959 </a>
|
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</span>
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</td>
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</tr>
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</tbody>
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</table>
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</div>
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</div>
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<div>
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<div class="btn-group ">
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<a href="/clinicalSynopsis/140000" class="btn btn-warning" role="button"> Clinical Synopsis </a>
|
|
<button type="button" id="mimPhenotypicSeriesToggle" class="btn btn-warning dropdown-toggle mimSingletonFoldToggle" data-toggle="collapse" href="#mimClinicalSynopsisFold" onclick="ga('send', 'event', 'Unfurl', 'ClinicalSynopsis', 'omim.org')">
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<span class="caret"></span>
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<span class="sr-only">Toggle Dropdown</span>
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</button>
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</div>
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<div class="btn-group">
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<button type="button" class="btn btn-success dropdown-toggle" data-toggle="dropdown" aria-haspopup="true" aria-expanded="false">
|
|
PheneGene Graphics <span class="caret"></span>
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</button>
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<ul class="dropdown-menu" style="width: 17em;">
|
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<li><a href="/graph/linear/140000" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Linear'})"> Linear </a></li>
|
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<li><a href="/graph/radial/140000" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Radial'})"> Radial </a></li>
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</ul>
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</div>
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<span class="glyphicon glyphicon-question-sign mim-tip-hint" title="OMIM PheneGene graphics depict relationships between phenotypes, groups of related phenotypes (Phenotypic Series), and genes.<br /><a href='/static/omim/pdf/OMIM_Graphics.pdf' target='_blank'>A quick reference overview and guide (PDF)</a>"></span>
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<div>
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<p />
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</div>
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<div id="mimClinicalSynopsisFold" class="well well-sm collapse mimSingletonToggleFold">
|
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<div class="small" style="margin: 5px">
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<div>
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<div>
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<span class="h5 mim-font">
|
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<strong> INHERITANCE </strong>
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</span>
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</div>
|
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<div style="margin-left: 2em;">
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<div>
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<span class="mim-font">
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- Autosomal dominant <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/263681008" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">263681008</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/771269000" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">771269000</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0443147&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0443147</a>, <a href="https://bioportal.bioontology.org/search?q=C1867440&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1867440</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000006" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000006</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000006" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000006</a>]</span><br />
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</span>
|
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</div>
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</div>
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</div>
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<div>
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<div>
|
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<span class="h5 mim-font">
|
|
<strong> GENITOURINARY </strong>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
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<div>
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<div>
|
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<span class="h5 mim-font">
|
|
<em> External Genitalia (Male) </em>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
<span class="mim-font">
|
|
|
|
- Hypospadias <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/204888000" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">204888000</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/416010008" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">416010008</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/Q54.1" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">Q54.1</a>, <a href="https://purl.bioontology.org/ontology/ICD10CM/Q54.9" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">Q54.9</a>, <a href="https://purl.bioontology.org/ontology/ICD10CM/Q54" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">Q54</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/752.61" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">752.61</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0848558&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0848558</a>, <a href="https://bioportal.bioontology.org/search?q=C1691215&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1691215</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0003244" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0003244</a>, <a href="https://hpo.jax.org/app/browse/term/HP:0000047" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000047</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000047" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000047</a>]</span><br /> -
|
|
Short penis <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/34911001" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">34911001</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/Q55.62" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">Q55.62</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/752.64" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">752.64</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C4551492&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C4551492</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000054" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000054</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000054" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000054</a>]</span><br /> -
|
|
Chordee <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/4287008" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">4287008</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0221182&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0221182</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000041" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000041</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000041" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000041</a>]</span><br /> -
|
|
Bifid scrotum <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/236780002" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">236780002</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0341787&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0341787</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000048" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000048</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000048" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000048</a>]</span><br />
|
|
|
|
</span>
|
|
</div>
|
|
</div>
|
|
|
|
|
|
|
|
|
|
<div>
|
|
<div>
|
|
<span class="h5 mim-font">
|
|
<em> Internal Genitalia (Female) </em>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
<span class="mim-font">
|
|
|
|
- Longitudinal vaginal septum <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/Q52.12" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">Q52.12</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/752.47" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">752.47</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1841680&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1841680</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008740" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008740</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008740" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008740</a>]</span><br /> -
|
|
Double uterus <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/22504001" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">22504001</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/Q51.28" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">Q51.28</a>, <a href="https://purl.bioontology.org/ontology/ICD10CM/Q51.2" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">Q51.2</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/752.2" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">752.2</a>, <a href="https://purl.bioontology.org/ontology/ICD9CM/752.35" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">752.35</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0152240&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0152240</a>, <a href="https://bioportal.bioontology.org/search?q=C5671328&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C5671328</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0003762" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0003762</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0003762" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0003762</a>]</span><br /> -
|
|
Double cervix <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/58135005" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">58135005</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/248912003" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">248912003</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0425885&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0425885</a>]</span><br />
|
|
|
|
</span>
|
|
</div>
|
|
</div>
|
|
|
|
|
|
<div>
|
|
<div>
|
|
<span class="h5 mim-font">
|
|
<em> Kidneys </em>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
<span class="mim-font">
|
|
|
|
- Chronic pyelonephritis <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/63302006" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">63302006</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/N11" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">N11</a>, <a href="https://purl.bioontology.org/ontology/ICD10CM/N11.9" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">N11.9</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/590.0" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">590.0</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0085697&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0085697</a>]</span><br /> -
|
|
Renal insufficiency <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/723188008" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">723188008</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/42399005" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">42399005</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/236423003" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">236423003</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/N19" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">N19</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/586" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">586</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1565489&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1565489</a>, <a href="https://bioportal.bioontology.org/search?q=C0035078&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0035078</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000083" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000083</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000083" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000083</a>]</span><br /> -
|
|
Renal transplant <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/70536003" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">70536003</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/55.6" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">55.6</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0022671&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0022671</a>]</span><br />
|
|
|
|
</span>
|
|
</div>
|
|
</div>
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|
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|
|
<div>
|
|
<div>
|
|
<span class="h5 mim-font">
|
|
<em> Ureters </em>
|
|
</span>
|
|
</div>
|
|
<div style="margin-left: 2em;">
|
|
<span class="mim-font">
|
|
|
|
- Vesicoureteral reflux <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/197811007" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">197811007</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/N13.70" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">N13.70</a>, <a href="https://purl.bioontology.org/ontology/ICD10CM/N13.7" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">N13.7</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/593.7" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">593.7</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0042580&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0042580</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000076" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000076</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000076" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000076</a>]</span><br /> -
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Ureteropelvic junction obstruction <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/95575002" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">95575002</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/Q62.39" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">Q62.39</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0521619&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0521619</a>, <a href="https://bioportal.bioontology.org/search?q=C5574705&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C5574705</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000074" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000074</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000074" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000074</a>]</span><br />
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</span>
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</div>
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</div>
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</div>
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</div>
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<div>
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<div>
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<span class="h5 mim-font">
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<strong> SKELETAL </strong>
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</span>
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</div>
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<div style="margin-left: 2em;">
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<div>
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<div>
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<span class="h5 mim-font">
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<em> Hands </em>
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</span>
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</div>
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<div style="margin-left: 2em;">
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<span class="mim-font">
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- Short thumbs <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/253936008" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">253936008</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0431890&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0431890</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0009778" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0009778</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0009778" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0009778</a>]</span><br /> -
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Proximally placed thumbs <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1865572&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1865572</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0009623" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0009623</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0009623" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0009623</a>]</span><br /> -
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Hypoplastic thenar eminences <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1846474&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1846474</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0001245" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0001245</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0001245" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0001245</a>]</span><br /> -
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Second finger ulnar deviation <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1844891&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1844891</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0009464" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0009464</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0009464" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0009464</a>]</span><br /> -
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Fifth finger clinodactyly <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1850049&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1850049</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0004209" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0004209</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0004209" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0004209</a>]</span><br /> -
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Fifth finger brachydactyly <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1842878&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1842878</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0009237" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0009237</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0009237" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0009237</a>]</span><br /> -
|
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Carpal delayed ossification <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1841684&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1841684</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0001216" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0001216</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0001216" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0001216</a>]</span><br /> -
|
|
Short first metacarpal <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1849311&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1849311</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0010034" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0010034</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0010034" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0010034</a>]</span><br /> -
|
|
Hypoplastic middle phalanges <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1846950&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1846950</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0005819" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0005819</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0005819" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0005819</a>]</span><br /> -
|
|
Pseudoepiphyses <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1841685&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1841685</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0010584" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0010584</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0010584" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0010584</a>]</span><br />
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</span>
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</div>
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</div>
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<div>
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<div>
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<span class="h5 mim-font">
|
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<em> Feet </em>
|
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</span>
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</div>
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<div style="margin-left: 2em;">
|
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<span class="mim-font">
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- Absent halluces <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1841686&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1841686</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0012386" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0012386</a>]</span><br /> -
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Short halluces <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1865992&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1865992</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0010109" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0010109</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0010109" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0010109</a>]</span><br /> -
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Medially deviated halluces <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/274147008" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">274147008</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0546297&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0546297</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008080" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008080</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008080" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008080</a>]</span><br /> -
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Brachydactyly (2nd-5th toes) <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1857517&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1857517</a>]</span> <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/43476002" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">43476002</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0001156" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0001156</a>]</span><br /> -
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Tarsal delayed ossification <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1846853&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1846853</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008103" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008103</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0008103" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0008103</a>]</span><br /> -
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Short first metatarsal <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1841688&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1841688</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0010105" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0010105</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0010105" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0010105</a>]</span><br /> -
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|
Hypoplastic distal and middle phalanges <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1844927&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1844927</a>]</span><br /> -
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Fused cuneiforms <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1841689&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1841689</a>]</span><br />
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</span>
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</div>
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</div>
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</div>
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</div>
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<div>
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<div>
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<span class="h5 mim-font">
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<strong> MOLECULAR BASIS </strong>
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</span>
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</div>
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<div style="margin-left: 2em;">
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<div>
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<span class="mim-font">
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- Caused by mutation in the homeobox A13 gene (HOXA13, <a href="/entry/142959#0001">142959.0001</a>)<br />
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</span>
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</div>
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</div>
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</div>
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<div class="text-right">
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<a href="#mimClinicalSynopsisFold" data-toggle="collapse">▲ Close</a>
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</div>
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</div>
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</div>
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</div>
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<div>
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<br />
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</div>
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<div>
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<a id="text" class="mim-anchor"></a>
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<h4 href="#mimTextFold" id="mimTextToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
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<span id="mimTextToggleTriangle" class="small mimTextToggleTriangle">▼</span>
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<span class="mim-font">
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<span class="mim-tip-floating" qtip_title="<strong>Looking For More References?</strong>" qtip_text="Click the 'reference plus' icon <span class='glyphicon glyphicon-plus-sign'></span> at the end of each OMIM text paragraph to see more references related to the content of the preceding paragraph.">
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<strong>TEXT</strong>
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</span>
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</span>
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</h4>
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<div id="mimTextFold" class="collapse in ">
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<span class="mim-text-font">
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<p>A number sign (#) is used with this entry because of evidence that hand-foot-genital syndrome (HFG) is caused by heterozygous mutation in the HOXA13 gene (<a href="/entry/142959">142959</a>) on chromosome 7p15.</p>
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</span>
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<div>
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<br />
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</div>
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</div>
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<p>Hand-foot-genital syndrome (HFGS) is an autosomal dominant condition characterized by distal limb and distal genitourinary tract malformations. The most striking limb abnormality is first-digit hypoplasia, comprising short, proximally placed thumbs with hypoplastic thenar eminences and short, medially deviated halluces. There is also ulnar deviation of the second fingers, clinodactyly/brachydactyly of the fifth fingers, brachydactyly of the second to fifth toes, and delayed ossification, fusion, and shortening of the carpals and tarsals. These abnormalities appear to be fully penetrant, bilateral, and symmetrical, with little variation in severity. In contrast, genitourinary tract abnormalities are incompletely penetrant and variably severe, and include hypospadias in males, Mullerian duct fusion defects in females, vesicoureteric reflux, and pelviureteric junction obstruction (summary by <a href="#6" class="mim-tip-reference" title="Goodman, F. R., Bacchelli, C., Brady, A. F., Brueton, L. A., Fryns, J.-P., Mortlock, D. P., Innis, J. W., Holmes, L. B., Donnenfeld, A. E., Feingold, M., Beemer, F. A., Hennekam, R. C. M., Scambler, P. J. <strong>Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.</strong> Am. J. Hum. Genet. 67: 197-202, 2000.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10839976/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10839976</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/?term=10839976[PMID]&report=imagesdocsum" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Image', 'domain': 'ncbi.nlm.nih.gov'})">images</a>] [<a href="https://doi.org/10.1086/302961" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="10839976">Goodman et al., 2000</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10839976" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<p>The clinical features include small feet with unusually short great toes and abnormal thumbs. Females with the disorder have duplication of the genital tract, including longitudinal vaginal septum (<a href="#14" class="mim-tip-reference" title="Stern, A. M., Gall, J. C., Jr., Perry, B. L., Stimson, C. W., Weitkamp, L. R., Poznanski, A. K. <strong>The hand-foot-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract.</strong> J. Pediat. 77: 109-116, 1970.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/5450271/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">5450271</a>] [<a href="https://doi.org/10.1016/s0022-3476(70)80052-x" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="5450271">Stern et al., 1970</a>). The radiographic changes were reviewed by <a href="#13" class="mim-tip-reference" title="Poznanski, A. K., Stern, A. M., Gall, J. C., Jr. <strong>Radiographic findings in the hand-foot-uterus syndrome (HFUS).</strong> Radiology 95: 129-134, 1970.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/5417032/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">5417032</a>] [<a href="https://doi.org/10.1148/95.1.129" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="5417032">Poznanski et al. (1970)</a>, who suggested that there is a typical metacarpophalangeal profile pattern. The changes included short first metacarpal and metatarsal, short fifth fingers with clinodactyly, trapezium-scaphoid fusion in the wrist, and cuneiform-navicular fusion in the foot. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=5417032+5450271" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#12" class="mim-tip-reference" title="Poznanski, A. K., Kuhns, L. R., Lapides, J., Stern, A. M. <strong>A new family with the hand-foot-genital syndrome--a wider spectrum of the hand-foot-uterus syndrome.</strong> Birth Defects Orig. Art. Ser. 11(4): 127-135, 1975.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/1156681/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">1156681</a>]" pmid="1156681">Poznanski et al. (1975)</a> described another kindred with this disorder. The pattern of radiologic changes in the hands and feet were sufficiently characteristic to suggest the diagnosis when the proband, a girl less than 4 years old, was admitted for evaluation of urinary incontinence and recurrent urinary tract infection. This was the prototype for one of the 'phenotypic communities of human malformation syndromes' discussed by <a href="#11" class="mim-tip-reference" title="Pinsky, L. <strong>A community of human malformation syndromes involving the mullerian ducts, distal extremities, urinary tract, and ears.</strong> Teratology 9: 65-80, 1974.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/4855855/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">4855855</a>] [<a href="https://doi.org/10.1002/tera.1420090109" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="4855855">Pinsky (1974)</a>. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=1156681+4855855" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#3" class="mim-tip-reference" title="Elias, S., Simpson, J. L., Feingold, M., Sarto, G. E. <strong>The hand-foot-uterus syndrome: a rare autosomal dominant disorder. (Abstract)</strong> Fertil. Steril. 29: 239-240, 1978."None>Elias et al. (1978)</a> investigated a third family in which 5 females in 3 generations were affected. The proband was a 17-year-old girl with strabismus, hypoplastic thenar eminences, malformed thumbs, bilateral fifth finger clinodactyly, short halluces, uterus bicornis bicollis, longitudinal vaginal septum and bilateral ureterovesical reflux.</p><p><a href="#7" class="mim-tip-reference" title="Halal, F. <strong>The hand-foot-genital (hand-foot-uterus) syndrome: family report and update.</strong> Am. J. Med. Genet. 30: 793-803, 1988.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/3189398/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">3189398</a>] [<a href="https://doi.org/10.1002/ajmg.1320300312" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="3189398">Halal (1988)</a> described a family in which affected females had urologic abnormalities. At least 3 affected males had penile hypospadias with chordee. A fourth, who had not been married, had a surgical operation on the genitalia at age 45, but the type of surgery was not known. Hypoplastic thenar eminences, 'stubby' thumbs, 5th finger clinodactyly, and short great toes were commented on. One affected female in this family had hypospadiac urethra and ectopic accessory ureteral orifice, with recurrent urinary tract infections leading to chronic pyelonephritis, renal insufficiency, and kidney transplantation. <a href="#16" class="mim-tip-reference" title="Verp, M. S. <strong>Urinary tract abnormalities in hand-foot-genital syndrome. (Letter)</strong> Am. J. Med. Genet. 32: 555 only, 1989.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2774004/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2774004</a>] [<a href="https://doi.org/10.1002/ajmg.1320320429" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="2774004">Verp (1989)</a> corroborated the significance of urologic abnormalities as part of this syndrome in females. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=3189398+2774004" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#8" class="mim-tip-reference" title="Hennekam, R. C. M. <strong>Acral-genital anomalies combined with ear anomalies. (Letter)</strong> Am. J. Med. Genet. 34: 454-455, 1989.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2596533/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2596533</a>] [<a href="https://doi.org/10.1002/ajmg.1320340325" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="2596533">Hennekam (1989)</a> pointed out 2 other reports of this syndrome and reported a kindred with autosomal dominant inheritance. Complete duplication of the genital tract including a longitudinal vaginal septum was expressed in 3 females. The diagnosis of HFG syndrome was not completely certain because there were no hand anomalies or typical metacarpophalangeal profile pattern. An additional feature was the presence of external ear anomalies; 6 members of the family had small ears with thickened, dysplastic helices. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=2596533" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#15" class="mim-tip-reference" title="Verp, M. S., Simpson, J. L., Elias, S., Carson, S. A., Sarto, G. E., Feingold, M. <strong>Heritable aspects of uterine anomalies. I. Three familial aggregates with mullerian fusion anomalies.</strong> Fertil. Steril. 40: 80-85, 1983.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/6862042/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">6862042</a>] [<a href="https://doi.org/10.1016/s0015-0282(16)47181-5" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="6862042">Verp et al. (1983)</a> reported a family in which 5 affected individuals in 3 generations, all female, had hand and foot anomalies consisting of short thumbs with hypoplastic distal phalanges, brachyclinodactyly V, bilateral hypoplasia and medial deviation of the distal halluces, and clinodactyly of the fifth toes. In 2 of the 5 women who were thoroughly evaluated, incomplete mullerian fusion defects were found. The proposita had presented with recurrent urinary tract infections due to bilateral vesicoureteral reflux at age 2 years. <a href="#2" class="mim-tip-reference" title="Donnenfeld, A. E., Schrager, D. S., Corson, S. L. <strong>Update on a family with hand-foot-genital syndrome: hypospadias and urinary tract abnormalities in two boys from the fourth generation.</strong> Am. J. Med. Genet. 44: 482-484, 1992.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/1442892/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">1442892</a>] [<a href="https://doi.org/10.1002/ajmg.1320440419" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="1442892">Donnenfeld et al. (1992)</a> reported on the same family, studied when the proposita presented at 19 years of age in premature labor at 22 weeks of gestation due to her uterine anomaly. They documented the genitourinary abnormalities in her 2 affected sisters, not previously examined, and documented hypospadias and urinary tract anomalies in 2 males from the fourth generation. One of the boys had bilateral vesicoureteral reflux and the other had bilateral ureteropelvic junction obstruction. Hypospadias is a manifestation of the disorder in males (<a href="#5" class="mim-tip-reference" title="Giedion, A., Prader, A. <strong>Hand-foot-uterus (HFU) syndrome with hypospadias: the hand-foot-genital (HFG) syndrome.</strong> Pediat. Radiol. 4: 96-102, 1976.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/987572/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">987572</a>] [<a href="https://doi.org/10.1007/BF00973951" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="987572">Giedion and Prader, 1976</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?term=1442892+6862042+987572" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#1" class="mim-tip-reference" title="Cleveland, R. H., Holmes, L. B. <strong>Hand-foot-genital syndrome: the importance of hallux varus.</strong> Pediat. Radiol. 20: 339-343, 1990.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2349017/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2349017</a>] [<a href="https://doi.org/10.1007/BF02013170" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="2349017">Cleveland and Holmes (1990)</a> emphasized the importance of hallux varus in the diagnosis. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=2349017" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<p><a href="#8" class="mim-tip-reference" title="Hennekam, R. C. M. <strong>Acral-genital anomalies combined with ear anomalies. (Letter)</strong> Am. J. Med. Genet. 34: 454-455, 1989.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2596533/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2596533</a>] [<a href="https://doi.org/10.1002/ajmg.1320340325" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="2596533">Hennekam (1989)</a> reported a kindred with autosomal dominant inheritance of HFG. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=2596533" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#4" class="mim-tip-reference" title="Fryns, J. P., Vogels, A., Decock, P., van den Berghe, H. <strong>The hand-foot-genital syndrome: on the variable expression in affected males.</strong> Clin. Genet. 43: 232-234, 1993.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8375102/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8375102</a>] [<a href="https://doi.org/10.1111/j.1399-0004.1993.tb03808.x" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="8375102">Fryns et al. (1993)</a> documented male-to-male transmission. An affected father begot 3 affected sons. A grade IV hypospadias, which was the most severe genital anomaly, was present in the youngest, moderately mentally retarded microcephalic male sib. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8375102" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<p>On the basis of update and linkage analysis of the family reported by <a href="#14" class="mim-tip-reference" title="Stern, A. M., Gall, J. C., Jr., Perry, B. L., Stimson, C. W., Weitkamp, L. R., Poznanski, A. K. <strong>The hand-foot-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract.</strong> J. Pediat. 77: 109-116, 1970.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/5450271/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">5450271</a>] [<a href="https://doi.org/10.1016/s0022-3476(70)80052-x" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="5450271">Stern et al. (1970)</a>, <a href="#10" class="mim-tip-reference" title="Mortlock, D. P. <strong>Personal Communication.</strong> Ann Arbor, Mich. 10/31/1996."None>Mortlock (1996)</a> and his colleagues demonstrated mutation in the HOXA13 gene (<a href="/entry/142959">142959</a>) as the cause of the hand-foot-uterus syndrome. Affected members of the family reported by <a href="#14" class="mim-tip-reference" title="Stern, A. M., Gall, J. C., Jr., Perry, B. L., Stimson, C. W., Weitkamp, L. R., Poznanski, A. K. <strong>The hand-foot-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract.</strong> J. Pediat. 77: 109-116, 1970.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/5450271/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">5450271</a>] [<a href="https://doi.org/10.1016/s0022-3476(70)80052-x" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="5450271">Stern et al. (1970)</a> showed a nonsense mutation (<a href="/entry/142959#0001">142959.0001</a>) which converted a highly conserved tryptophan residue in the homeodomain of HOXA13 to a stop codon and truncated 20 amino acids from the protein (<a href="#9" class="mim-tip-reference" title="Mortlock, D. P., Innis, J. W. <strong>Mutation of HOXA13 in hand-foot-genital syndrome.</strong> Nature Genet. 15: 179-181, 1997.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9020844/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9020844</a>] [<a href="https://doi.org/10.1038/ng0297-179" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="9020844">Mortlock and Innis, 1997</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?term=5450271+9020844" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#6" class="mim-tip-reference" title="Goodman, F. R., Bacchelli, C., Brady, A. F., Brueton, L. A., Fryns, J.-P., Mortlock, D. P., Innis, J. W., Holmes, L. B., Donnenfeld, A. E., Feingold, M., Beemer, F. A., Hennekam, R. C. M., Scambler, P. J. <strong>Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.</strong> Am. J. Hum. Genet. 67: 197-202, 2000.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10839976/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10839976</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/?term=10839976[PMID]&report=imagesdocsum" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Image', 'domain': 'ncbi.nlm.nih.gov'})">images</a>] [<a href="https://doi.org/10.1086/302961" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="10839976">Goodman et al. (2000)</a> examined the HOXA13 gene in 2 new and 4 previously reported families with features of HFG syndrome and identified heterozygous mutations in 5 families (see, e.g., <a href="/entry/142959#0002">142959.0002</a>-<a href="/entry/142959#0004">142959.0004</a>). In 3 families, nonsense mutations truncating the encoded protein N-terminal to or within the homeodomain produced typical limb and genitourinary abnormalities; in the fourth family, an expansion of an N-terminal polyalanine tract produced a similar phenotype; in the fifth family, a missense mutation, which altered an invariant domain, produced an exceptionally severe limb phenotype. In the sixth family, first reported by <a href="#8" class="mim-tip-reference" title="Hennekam, R. C. M. <strong>Acral-genital anomalies combined with ear anomalies. (Letter)</strong> Am. J. Med. Genet. 34: 454-455, 1989.[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2596533/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2596533</a>] [<a href="https://doi.org/10.1002/ajmg.1320340325" target="_blank" onclick="gtag('event', 'mim_outbound', {'destination': 'Publisher'})">Full Text</a>]" pmid="2596533">Hennekam (1989)</a>, in which limb abnormalities were atypical, no HOXA13 mutation was detected. In all families in which a mutation was detected, the limb abnormalities were fully penetrant, bilateral, and symmetrical, with analogous involvement of the hands and feet. In contrast, genitourinary abnormalities were incompletely penetrant and variably severe. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=2596533+10839976" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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[<a href="https://doi.org/10.1002/ajmg.1320440419" target="_blank">Full Text</a>]
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[<a href="https://doi.org/10.1111/j.1399-0004.1993.tb03808.x" target="_blank">Full Text</a>]
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/987572/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">987572</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=987572" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1007/BF00973951" target="_blank">Full Text</a>]
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Goodman, F. R., Bacchelli, C., Brady, A. F., Brueton, L. A., Fryns, J.-P., Mortlock, D. P., Innis, J. W., Holmes, L. B., Donnenfeld, A. E., Feingold, M., Beemer, F. A., Hennekam, R. C. M., Scambler, P. J.
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<strong>Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.</strong>
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Am. J. Hum. Genet. 67: 197-202, 2000.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/10839976/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">10839976</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/?term=10839976[PMID]&report=imagesdocsum" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Image', 'domain': 'ncbi.nlm.nih.gov'})">images</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=10839976" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1086/302961" target="_blank">Full Text</a>]
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/3189398/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">3189398</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=3189398" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1002/ajmg.1320300312" target="_blank">Full Text</a>]
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<a id="Hennekam1989" class="mim-anchor"></a>
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<div class="">
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Hennekam, R. C. M.
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<strong>Acral-genital anomalies combined with ear anomalies. (Letter)</strong>
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Am. J. Med. Genet. 34: 454-455, 1989.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2596533/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2596533</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=2596533" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1002/ajmg.1320340325" target="_blank">Full Text</a>]
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<a id="Mortlock1997" class="mim-anchor"></a>
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Mortlock, D. P., Innis, J. W.
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<strong>Mutation of HOXA13 in hand-foot-genital syndrome.</strong>
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Nature Genet. 15: 179-181, 1997.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/9020844/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">9020844</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=9020844" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1038/ng0297-179" target="_blank">Full Text</a>]
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/4855855/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">4855855</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=4855855" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1002/tera.1420090109" target="_blank">Full Text</a>]
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Poznanski, A. K., Kuhns, L. R., Lapides, J., Stern, A. M.
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<strong>A new family with the hand-foot-genital syndrome--a wider spectrum of the hand-foot-uterus syndrome.</strong>
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/1156681/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">1156681</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=1156681" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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Poznanski, A. K., Stern, A. M., Gall, J. C., Jr.
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<strong>Radiographic findings in the hand-foot-uterus syndrome (HFUS).</strong>
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Radiology 95: 129-134, 1970.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/5417032/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">5417032</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=5417032" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1148/95.1.129" target="_blank">Full Text</a>]
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Stern, A. M., Gall, J. C., Jr., Perry, B. L., Stimson, C. W., Weitkamp, L. R., Poznanski, A. K.
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<strong>The hand-foot-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract.</strong>
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J. Pediat. 77: 109-116, 1970.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/5450271/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">5450271</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=5450271" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1016/s0022-3476(70)80052-x" target="_blank">Full Text</a>]
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Verp, M. S., Simpson, J. L., Elias, S., Carson, S. A., Sarto, G. E., Feingold, M.
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<strong>Heritable aspects of uterine anomalies. I. Three familial aggregates with mullerian fusion anomalies.</strong>
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/6862042/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">6862042</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=6862042" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1016/s0015-0282(16)47181-5" target="_blank">Full Text</a>]
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Verp, M. S.
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<strong>Urinary tract abnormalities in hand-foot-genital syndrome. (Letter)</strong>
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Am. J. Med. Genet. 32: 555 only, 1989.
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[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/2774004/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">2774004</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=2774004" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
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[<a href="https://doi.org/10.1002/ajmg.1320320429" target="_blank">Full Text</a>]
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Anne M. Stumpf - updated : 03/09/2020
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Kelly A. Przylepa - updated : 2/18/2005
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Victor A. McKusick : 6/4/1986
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carol : 03/10/2020
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alopez : 03/09/2020<br>joanna : 04/18/2014<br>carol : 11/12/2013<br>joanna : 12/31/2008<br>terry : 9/25/2008<br>wwang : 2/28/2005<br>terry : 2/18/2005<br>mark : 2/2/1997<br>terry : 1/31/1997<br>terry : 1/29/1997<br>terry : 11/22/1996<br>terry : 11/21/1996<br>mimadm : 9/24/1994<br>davew : 7/20/1994<br>terry : 5/9/1994<br>carol : 11/5/1993<br>carol : 6/7/1993<br>carol : 5/7/1993
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<strong>#</strong> 140000
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HAND-FOOT-GENITAL SYNDROME; HFG
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HAND-FOOT-UTERUS SYNDROME; HFU
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<strong>SNOMEDCT:</strong> 702425002;
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<strong>ORPHA:</strong> 2438;
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<strong>DO:</strong> 0060739;
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<strong>Phenotype-Gene Relationships</strong>
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Phenotype
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Phenotype <br /> MIM number
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Inheritance
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Phenotype <br /> mapping key
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7p15.2
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<span class="mim-font">
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Hand-foot-genital syndrome
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140000
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Autosomal dominant
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3
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HOXA13
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142959
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<p>A number sign (#) is used with this entry because of evidence that hand-foot-genital syndrome (HFG) is caused by heterozygous mutation in the HOXA13 gene (142959) on chromosome 7p15.</p>
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<strong>Description</strong>
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<p>Hand-foot-genital syndrome (HFGS) is an autosomal dominant condition characterized by distal limb and distal genitourinary tract malformations. The most striking limb abnormality is first-digit hypoplasia, comprising short, proximally placed thumbs with hypoplastic thenar eminences and short, medially deviated halluces. There is also ulnar deviation of the second fingers, clinodactyly/brachydactyly of the fifth fingers, brachydactyly of the second to fifth toes, and delayed ossification, fusion, and shortening of the carpals and tarsals. These abnormalities appear to be fully penetrant, bilateral, and symmetrical, with little variation in severity. In contrast, genitourinary tract abnormalities are incompletely penetrant and variably severe, and include hypospadias in males, Mullerian duct fusion defects in females, vesicoureteric reflux, and pelviureteric junction obstruction (summary by Goodman et al., 2000). </p>
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<p>The clinical features include small feet with unusually short great toes and abnormal thumbs. Females with the disorder have duplication of the genital tract, including longitudinal vaginal septum (Stern et al., 1970). The radiographic changes were reviewed by Poznanski et al. (1970), who suggested that there is a typical metacarpophalangeal profile pattern. The changes included short first metacarpal and metatarsal, short fifth fingers with clinodactyly, trapezium-scaphoid fusion in the wrist, and cuneiform-navicular fusion in the foot. </p><p>Poznanski et al. (1975) described another kindred with this disorder. The pattern of radiologic changes in the hands and feet were sufficiently characteristic to suggest the diagnosis when the proband, a girl less than 4 years old, was admitted for evaluation of urinary incontinence and recurrent urinary tract infection. This was the prototype for one of the 'phenotypic communities of human malformation syndromes' discussed by Pinsky (1974). </p><p>Elias et al. (1978) investigated a third family in which 5 females in 3 generations were affected. The proband was a 17-year-old girl with strabismus, hypoplastic thenar eminences, malformed thumbs, bilateral fifth finger clinodactyly, short halluces, uterus bicornis bicollis, longitudinal vaginal septum and bilateral ureterovesical reflux.</p><p>Halal (1988) described a family in which affected females had urologic abnormalities. At least 3 affected males had penile hypospadias with chordee. A fourth, who had not been married, had a surgical operation on the genitalia at age 45, but the type of surgery was not known. Hypoplastic thenar eminences, 'stubby' thumbs, 5th finger clinodactyly, and short great toes were commented on. One affected female in this family had hypospadiac urethra and ectopic accessory ureteral orifice, with recurrent urinary tract infections leading to chronic pyelonephritis, renal insufficiency, and kidney transplantation. Verp (1989) corroborated the significance of urologic abnormalities as part of this syndrome in females. </p><p>Hennekam (1989) pointed out 2 other reports of this syndrome and reported a kindred with autosomal dominant inheritance. Complete duplication of the genital tract including a longitudinal vaginal septum was expressed in 3 females. The diagnosis of HFG syndrome was not completely certain because there were no hand anomalies or typical metacarpophalangeal profile pattern. An additional feature was the presence of external ear anomalies; 6 members of the family had small ears with thickened, dysplastic helices. </p><p>Verp et al. (1983) reported a family in which 5 affected individuals in 3 generations, all female, had hand and foot anomalies consisting of short thumbs with hypoplastic distal phalanges, brachyclinodactyly V, bilateral hypoplasia and medial deviation of the distal halluces, and clinodactyly of the fifth toes. In 2 of the 5 women who were thoroughly evaluated, incomplete mullerian fusion defects were found. The proposita had presented with recurrent urinary tract infections due to bilateral vesicoureteral reflux at age 2 years. Donnenfeld et al. (1992) reported on the same family, studied when the proposita presented at 19 years of age in premature labor at 22 weeks of gestation due to her uterine anomaly. They documented the genitourinary abnormalities in her 2 affected sisters, not previously examined, and documented hypospadias and urinary tract anomalies in 2 males from the fourth generation. One of the boys had bilateral vesicoureteral reflux and the other had bilateral ureteropelvic junction obstruction. Hypospadias is a manifestation of the disorder in males (Giedion and Prader, 1976). </p><p>Cleveland and Holmes (1990) emphasized the importance of hallux varus in the diagnosis. </p>
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<span class="mim-font">
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<strong>Inheritance</strong>
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<p>Hennekam (1989) reported a kindred with autosomal dominant inheritance of HFG. </p><p>Fryns et al. (1993) documented male-to-male transmission. An affected father begot 3 affected sons. A grade IV hypospadias, which was the most severe genital anomaly, was present in the youngest, moderately mentally retarded microcephalic male sib. </p>
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<span class="mim-font">
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<strong>Molecular Genetics</strong>
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<p>On the basis of update and linkage analysis of the family reported by Stern et al. (1970), Mortlock (1996) and his colleagues demonstrated mutation in the HOXA13 gene (142959) as the cause of the hand-foot-uterus syndrome. Affected members of the family reported by Stern et al. (1970) showed a nonsense mutation (142959.0001) which converted a highly conserved tryptophan residue in the homeodomain of HOXA13 to a stop codon and truncated 20 amino acids from the protein (Mortlock and Innis, 1997). </p><p>Goodman et al. (2000) examined the HOXA13 gene in 2 new and 4 previously reported families with features of HFG syndrome and identified heterozygous mutations in 5 families (see, e.g., 142959.0002-142959.0004). In 3 families, nonsense mutations truncating the encoded protein N-terminal to or within the homeodomain produced typical limb and genitourinary abnormalities; in the fourth family, an expansion of an N-terminal polyalanine tract produced a similar phenotype; in the fifth family, a missense mutation, which altered an invariant domain, produced an exceptionally severe limb phenotype. In the sixth family, first reported by Hennekam (1989), in which limb abnormalities were atypical, no HOXA13 mutation was detected. In all families in which a mutation was detected, the limb abnormalities were fully penetrant, bilateral, and symmetrical, with analogous involvement of the hands and feet. In contrast, genitourinary abnormalities were incompletely penetrant and variably severe. </p>
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<span class="mim-font">
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<strong>REFERENCES</strong>
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</h4>
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<div>
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<p class="mim-text-font">
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Cleveland, R. H., Holmes, L. B.
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<strong>Hand-foot-genital syndrome: the importance of hallux varus.</strong>
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Pediat. Radiol. 20: 339-343, 1990.
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[PubMed: 2349017]
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[Full Text: https://doi.org/10.1007/BF02013170]
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Donnenfeld, A. E., Schrager, D. S., Corson, S. L.
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<strong>Update on a family with hand-foot-genital syndrome: hypospadias and urinary tract abnormalities in two boys from the fourth generation.</strong>
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Am. J. Med. Genet. 44: 482-484, 1992.
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[PubMed: 1442892]
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[Full Text: https://doi.org/10.1002/ajmg.1320440419]
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<li>
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<p class="mim-text-font">
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Elias, S., Simpson, J. L., Feingold, M., Sarto, G. E.
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<strong>The hand-foot-uterus syndrome: a rare autosomal dominant disorder. (Abstract)</strong>
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Fertil. Steril. 29: 239-240, 1978.
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</p>
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</li>
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<p class="mim-text-font">
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Fryns, J. P., Vogels, A., Decock, P., van den Berghe, H.
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<strong>The hand-foot-genital syndrome: on the variable expression in affected males.</strong>
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Clin. Genet. 43: 232-234, 1993.
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[PubMed: 8375102]
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[Full Text: https://doi.org/10.1111/j.1399-0004.1993.tb03808.x]
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<li>
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<p class="mim-text-font">
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Giedion, A., Prader, A.
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<strong>Hand-foot-uterus (HFU) syndrome with hypospadias: the hand-foot-genital (HFG) syndrome.</strong>
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Pediat. Radiol. 4: 96-102, 1976.
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[PubMed: 987572]
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[Full Text: https://doi.org/10.1007/BF00973951]
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<p class="mim-text-font">
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Goodman, F. R., Bacchelli, C., Brady, A. F., Brueton, L. A., Fryns, J.-P., Mortlock, D. P., Innis, J. W., Holmes, L. B., Donnenfeld, A. E., Feingold, M., Beemer, F. A., Hennekam, R. C. M., Scambler, P. J.
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<strong>Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.</strong>
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Am. J. Hum. Genet. 67: 197-202, 2000.
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[PubMed: 10839976]
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[Full Text: https://doi.org/10.1086/302961]
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<p class="mim-text-font">
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Halal, F.
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<strong>The hand-foot-genital (hand-foot-uterus) syndrome: family report and update.</strong>
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Am. J. Med. Genet. 30: 793-803, 1988.
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[PubMed: 3189398]
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[Full Text: https://doi.org/10.1002/ajmg.1320300312]
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</p>
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</li>
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<li>
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<p class="mim-text-font">
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Hennekam, R. C. M.
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<strong>Acral-genital anomalies combined with ear anomalies. (Letter)</strong>
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Am. J. Med. Genet. 34: 454-455, 1989.
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[PubMed: 2596533]
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[Full Text: https://doi.org/10.1002/ajmg.1320340325]
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</p>
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</li>
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<li>
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<p class="mim-text-font">
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Mortlock, D. P., Innis, J. W.
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<strong>Mutation of HOXA13 in hand-foot-genital syndrome.</strong>
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Nature Genet. 15: 179-181, 1997.
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[PubMed: 9020844]
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[Full Text: https://doi.org/10.1038/ng0297-179]
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</p>
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</li>
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<li>
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<p class="mim-text-font">
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Mortlock, D. P.
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<strong>Personal Communication.</strong>
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Ann Arbor, Mich. 10/31/1996.
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</p>
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</li>
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<li>
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<p class="mim-text-font">
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Pinsky, L.
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<strong>A community of human malformation syndromes involving the mullerian ducts, distal extremities, urinary tract, and ears.</strong>
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Teratology 9: 65-80, 1974.
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[PubMed: 4855855]
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[Full Text: https://doi.org/10.1002/tera.1420090109]
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</p>
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</li>
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<li>
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<p class="mim-text-font">
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Poznanski, A. K., Kuhns, L. R., Lapides, J., Stern, A. M.
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<strong>A new family with the hand-foot-genital syndrome--a wider spectrum of the hand-foot-uterus syndrome.</strong>
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Birth Defects Orig. Art. Ser. 11(4): 127-135, 1975.
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[PubMed: 1156681]
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</p>
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</li>
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<li>
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<p class="mim-text-font">
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Poznanski, A. K., Stern, A. M., Gall, J. C., Jr.
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<strong>Radiographic findings in the hand-foot-uterus syndrome (HFUS).</strong>
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Radiology 95: 129-134, 1970.
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[PubMed: 5417032]
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[Full Text: https://doi.org/10.1148/95.1.129]
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</p>
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</li>
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<li>
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Stern, A. M., Gall, J. C., Jr., Perry, B. L., Stimson, C. W., Weitkamp, L. R., Poznanski, A. K.
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<strong>The hand-foot-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract.</strong>
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J. Pediat. 77: 109-116, 1970.
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[PubMed: 5450271]
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[Full Text: https://doi.org/10.1016/s0022-3476(70)80052-x]
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</p>
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</li>
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<li>
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<p class="mim-text-font">
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Verp, M. S., Simpson, J. L., Elias, S., Carson, S. A., Sarto, G. E., Feingold, M.
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<strong>Heritable aspects of uterine anomalies. I. Three familial aggregates with mullerian fusion anomalies.</strong>
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Fertil. Steril. 40: 80-85, 1983.
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[PubMed: 6862042]
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[Full Text: https://doi.org/10.1016/s0015-0282(16)47181-5]
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<li>
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<p class="mim-text-font">
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Verp, M. S.
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<strong>Urinary tract abnormalities in hand-foot-genital syndrome. (Letter)</strong>
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Am. J. Med. Genet. 32: 555 only, 1989.
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[PubMed: 2774004]
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[Full Text: https://doi.org/10.1002/ajmg.1320320429]
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Anne M. Stumpf - updated : 03/09/2020<br>Kelly A. Przylepa - updated : 2/18/2005
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Victor A. McKusick : 6/4/1986
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