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Entry
- %608652 - DEAFNESS, AUTOSOMAL DOMINANT 47; DFNA47
- OMIM
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<span class="h4">%608652</span>
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<a href="/clinicalSynopsis/608652"><strong>Clinical Synopsis</strong></a>
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<a href="#references"><strong>References</strong></a>
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<div id="mimGeneInfoLinksFold" class="panel-collapse collapse mimLinksFold" role="tabpanel">
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<div><a href="http://biogps.org/#goto=genereport&id=246289" class="mim-tip-hint" title="The Gene Portal Hub; customizable portal of gene and protein function information." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'BioGPS', 'domain': 'biogps.org'})">BioGPS</a></div>
<div><a href="https://www.genome.jp/dbget-bin/www_bget?hsa+246289" class="mim-tip-hint" title="Kyoto Encyclopedia of Genes and Genomes; diagrams of signaling pathways." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'KEGG', 'domain': 'genome.jp'})">KEGG</a></div>
<div><a href="https://www.ncbi.nlm.nih.gov/gene/246289" class="mim-tip-hint" title="Gene-specific map, sequence, expression, structure, function, citation, and homology data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Gene', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Gene</a></div>
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<div class="panel-heading mim-panel-heading" role="tab" id="mimClinicalResources">
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<div id="mimClinicalResourcesLinksToggleTriangle" class="small mimSingletonTriangle" style="color: #337CB5; display: table-cell;">&#9660;</div>
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<div><a href="https://clinicaltrials.gov/search?cond=DEAFNESS, AUTOSOMAL DOMINANT" 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>
<div><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=12046&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>
<div><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=90635" 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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<span>
<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.">
&nbsp;
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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">
<div>
<a id="title" class="mim-anchor"></a>
<div>
<a id="number" class="mim-anchor"></a>
<div class="text-right">
<a href="#" class="mim-tip-icd" qtip_title="<strong>ICD+</strong>" qtip_text="
<strong>ORPHA:</strong> 90635<br />
<strong>DO:</strong> 0110570<br />
">ICD+</a>
</div>
<div>
<span class="h3">
<span class="mim-font mim-tip-hint" title="Phenotype description or locus, molecular basis unknown">
<span class="text-danger"><strong>%</strong></span>
608652
</span>
</span>
</div>
</div>
<div>
<a id="preferredTitle" class="mim-anchor"></a>
<h3>
<span class="mim-font">
DEAFNESS, AUTOSOMAL DOMINANT 47; DFNA47
</span>
</h3>
</div>
<div>
<br />
</div>
</div>
<div>
<a id="cytogeneticLocation" class="mim-anchor"></a>
<p>
<span class="mim-text-font">
<strong>
<em>
Cytogenetic location: <a href="/geneMap/9/52?start=-3&limit=10&highlight=52">9p22-p21</a>
&nbsp;
Genomic coordinates <span class="small">(GRCh38)</span> : <a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&position=chr9:14200001-33200000&dgv=pack&knownGene=pack&omimGene=pack" class="mim-tip-hint" title="UCSC Genome Browser; reference sequences and working draft assemblies for a large collection of genomes." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'UCSC Genome Browser', 'domain': 'genome.ucsc.edu'})">9:14,200,001-33,200,000</a> </span>
</em>
</strong>
</span>
</p>
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<br />
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<a id="geneMap" class="mim-anchor"></a>
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<span class="h4 mim-font">
<strong>Gene-Phenotype Relationships</strong>
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<div>
<table class="table table-bordered table-condensed table-hover small mim-table-padding">
<thead>
<tr class="active">
<th>
Location
</th>
<th>
Phenotype
</th>
<th>
Phenotype <br /> MIM number
</th>
<th>
Inheritance
</th>
<th>
Phenotype <br /> mapping key
</th>
</tr>
</thead>
<tbody>
<tr>
<td rowspan="1">
<span class="mim-font">
<a href="/geneMap/9/52?start=-3&limit=10&highlight=52">
9p22-p21
</a>
</span>
</td>
<td>
<span class="mim-font">
Deafness, autosomal dominant 47
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> 608652 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods">2</abbr>
</span>
</td>
</tr>
</tbody>
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<a href="/clinicalSynopsis/608652" class="btn btn-warning" role="button"> Clinical Synopsis </a>
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PheneGene Graphics <span class="caret"></span>
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<ul class="dropdown-menu" style="width: 17em;">
<li><a href="/graph/linear/608652" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Linear'})"> Linear </a></li>
<li><a href="/graph/radial/608652" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Radial'})"> Radial </a></li>
</ul>
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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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<p />
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<div id="mimClinicalSynopsisFold" class="well well-sm collapse mimSingletonToggleFold">
<div class="small" style="margin: 5px">
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<span class="h5 mim-font">
<strong> INHERITANCE </strong>
</span>
</div>
<div style="margin-left: 2em;">
<div>
<span class="mim-font">
- 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 />
</span>
</div>
</div>
</div>
<div>
<div>
<span class="h5 mim-font">
<strong> HEAD & NECK </strong>
</span>
</div>
<div style="margin-left: 2em;">
<div>
<div>
<span class="h5 mim-font">
<em> Ears </em>
</span>
</div>
<div style="margin-left: 2em;">
<span class="mim-font">
- Hearing loss, progressive postlingual (in one Italian family) <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C4230289&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C4230289</a>]</span> <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/103276001" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">103276001</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/343087000" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">343087000</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/15188001" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">15188001</a>]</span> <span class="mim-feature-ids hidden">[ICD10CM: <a href="https://purl.bioontology.org/ontology/ICD10CM/H91.9" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD10CM\', \'domain\': \'bioontology.org\'})">H91.9</a>]</span> <span class="mim-feature-ids hidden">[ICD9CM: <a href="https://purl.bioontology.org/ontology/ICD9CM/389.9" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">389.9</a>, <a href="https://purl.bioontology.org/ontology/ICD9CM/389" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'ICD9CM\', \'domain\': \'bioontology.org\'})">389</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000365" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000365</a>]</span><br />
</span>
</div>
</div>
</div>
</div>
<div>
<div>
<span class="h5 mim-font">
<strong> MISCELLANEOUS </strong>
</span>
</div>
<div style="margin-left: 2em;">
<div>
<span class="mim-font">
- High frequency hearing loss progresses to include all frequencies<br /> -
Variable age of onset (20 to 35 years old)<br /> -
Based on one Italian family (last curated August 2015)<br />
</span>
</div>
</div>
</div>
<div class="text-right">
<a href="#mimClinicalSynopsisFold" data-toggle="collapse">&#9650;&nbsp;Close</a>
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<h5>
Deafness, autosomal dominant
- <a href="/phenotypicSeries/PS124900">PS124900</a>
- 75 Entries
</h5>
</div>
</div>
<div class="row" style="margin-left: 0.125em; margin-right: 0.125em;">
<table class="table table-bordered table-condensed table-hover mim-table-padding">
<thead>
<tr>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Location</strong>
</th>
<th class="col-lg-5 col-md-5 col-sm-5 col-xs-6 text-nowrap">
<strong>Phenotype</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Inheritance</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Phenotype<br />mapping key</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Phenotype<br />MIM number</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Gene/Locus</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Gene/Locus<br />MIM number</strong>
</th>
</tr>
</thead>
<tbody>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/253?start=-3&limit=10&highlight=253"> 1p36.12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620227"> Deafness, autosomal dominant 85 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620227"> 620227 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617445"> USP48 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617445"> 617445 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/423?start=-3&limit=10&highlight=423"> 1p34.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612644"> Deafness, autosomal dominant 2B, with or without peripheral neuropathy </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612644"> 612644 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603324"> GJB3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603324"> 603324 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/456?start=-3&limit=10&highlight=456"> 1p34.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620283"> ?Deafness, autosomal dominant 88 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620283"> 620283 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611123"> EPHA10 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611123"> 611123 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/495?start=-3&limit=10&highlight=495"> 1p34.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600101"> Deafness, autosomal dominant 2A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600101"> 600101 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603537"> KCNQ4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603537"> 603537 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/847?start=-3&limit=10&highlight=847"> 1p21.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618533"> Deafness, autosomal dominant 37 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618533"> 618533 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120280"> COL11A1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120280"> 120280 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/997?start=-3&limit=10&highlight=997"> 1q21-q23 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> Deafness, autosomal dominant 49 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> 608372 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> DFNA49 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> 608372 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1096?start=-3&limit=10&highlight=1096"> 1q21.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620281"> Deafness, autosomal dominant 87 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620281"> 620281 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602758"> PI4KB </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602758"> 602758 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1373?start=-3&limit=10&highlight=1373"> 1q23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601412"> Deafness, autosomal dominant 7 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601412"> 601412 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600298"> LMX1A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600298"> 600298 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1862?start=-3&limit=10&highlight=1862"> 1q44 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617772"> Deafness, autosomal dominant 34, with or without inflammation </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617772"> 617772 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606416"> NLRP3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606416"> 606416 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/205?start=-3&limit=10&highlight=205"> 2p21-p12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> Deafness, autosomal dominant 58 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="4 - A contiguous gene duplication or deletion syndrome in which multiple genes are involved"> 4 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> 615654 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> DFNA58 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> 615654 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/396?start=-3&limit=10&highlight=396"> 2p12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> Deafness, autosomal dominant 43 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> 608394 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> DFNA43 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> 608394 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/421?start=-3&limit=10&highlight=421"> 2p11.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619500"> ?Deafness, autosomal dominant 81 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619500"> 619500 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615427"> ELMOD3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615427"> 615427 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/675?start=-3&limit=10&highlight=675"> 2q23-q24.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> Deafness, autosomal dominant 16 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> 603964 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> DFNA16 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> 603964 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/58?start=-3&limit=10&highlight=58"> 3p25.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619804"> Deafness, autosomal dominant 82 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619804"> 619804 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/108733"> ATP2B2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/108733"> 108733 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/643?start=-3&limit=10&highlight=643"> 3q21.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616968"> ?Deafness, autosomal dominant 70 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616968"> 616968 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/116945"> MCM2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/116945"> 116945 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/665?start=-3&limit=10&highlight=665"> 3q22 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> Deafness, autosomal dominant 18 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> 606012 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> DFNA18 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> 606012 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/745?start=-3&limit=10&highlight=745"> 3q23 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618787"> Deafness, autosomal dominant 76 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618787"> 618787 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602734"> PLS1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602734"> 602734 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/966?start=-3&limit=10&highlight=966"> 3q28 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607453"> ?Deafness, autosomal dominant 44 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607453"> 607453 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611051"> CCDC50 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611051"> 611051 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/69?start=-3&limit=10&highlight=69"> 4p16.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600965"> Deafness, autosomal dominant 6/14/38 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600965"> 600965 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606201"> WFS1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606201"> 606201 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/243?start=-3&limit=10&highlight=243"> 4q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612431"> Deafness, autosomal dominant 27 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612431"> 612431 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600571"> REST </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600571"> 600571 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/365?start=-3&limit=10&highlight=365"> 4q21.22 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619086"> ?Deafness, autosomal dominant 79 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619086"> 619086 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608370"> SCD5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608370"> 608370 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/415?start=-3&limit=10&highlight=415"> 4q22.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620284"> ?Deafness, autosomal dominant 89 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620284"> 620284 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601461"> ATOH1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601461"> 601461 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/696?start=-3&limit=10&highlight=696"> 4q35-qter </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> Deafness, autosomal dominant 24 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> 606282 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> DFNA24 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> 606282 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/239?start=-3&limit=10&highlight=239"> 5q13.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619808"> ?Deafness, autosomal dominant 83 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619808"> 619808 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/157129"> MAP1B </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/157129"> 157129 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/412?start=-3&limit=10&highlight=412"> 5q23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619081"> Deafness, autosomal dominant 78 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619081"> 619081 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600840"> SLC12A2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600840"> 600840 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/424?start=-3&limit=10&highlight=424"> 5q31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> Deafness, autosomal dominant 54 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> 615649 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> DFNA54 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> 615649 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/605?start=-3&limit=10&highlight=605"> 5q31.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/124900"> Deafness, autosomal dominant 1, with or without thrombocytopenia </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/124900"> 124900 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602121"> DIAPH1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602121"> 602121 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/630?start=-3&limit=10&highlight=630"> 5q32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602459"> Deafness, autosomal dominant 15/52 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602459"> 602459 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602460"> POU4F3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602460"> 602460 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/119?start=-3&limit=10&highlight=119"> 6p22.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607017"> Deafness, autosomal dominant 21 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607017"> 607017 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611410"> RIPOR2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611410"> 611410 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/245?start=-3&limit=10&highlight=245"> 6p21.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> Deafness, autosomal dominant 31 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> 608645 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> DFNA31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> 608645 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/340?start=-3&limit=10&highlight=340"> 6p21.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617606"> ?Deafness, autosomal dominant 72 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617606"> 617606 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606107"> SLC44A4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606107"> 606107 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/383?start=-3&limit=10&highlight=383"> 6p21.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601868"> Deafness, autosomal dominant 13 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601868"> 601868 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120290"> COL11A2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120290"> 120290 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/658?start=-3&limit=10&highlight=658"> 6q14.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> Deafness, autosomal dominant 22 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> 606346 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> MYO6 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> 600970 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/658?start=-3&limit=10&highlight=658"> 6q14.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> 606346 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> MYO6 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> 600970 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/764?start=-3&limit=10&highlight=764"> 6q21 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616969"> ?Deafness, autosomal dominant 66 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616969"> 616969 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603356"> CD164 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603356"> 603356 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/874?start=-3&limit=10&highlight=874"> 6q23.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601316"> Deafness, autosomal dominant 10 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601316"> 601316 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603550"> EYA4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603550"> 603550 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/120?start=-3&limit=10&highlight=120"> 7p15.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600994"> Deafness, autosomal dominant 5 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600994"> 600994 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608798"> GSDME </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608798"> 608798 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/172?start=-3&limit=10&highlight=172"> 7p14.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618140"> ?Deafness, autosomal dominant 74 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618140"> 618140 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602987"> PDE1C </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602987"> 602987 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/457?start=-3&limit=10&highlight=457"> 7q22.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618778"> ?Deafness, autosomal dominant 75 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618778"> 618778 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603015"> TRRAP </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603015"> 603015 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/671?start=-3&limit=10&highlight=671"> 7q32.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613074"> Deafness, autosomal dominant 50 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613074"> 613074 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611606"> MIR96 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611606"> 611606 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/8/450?start=-3&limit=10&highlight=450"> 8q22.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608641"> Deafness, autosomal dominant 28 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608641"> 608641 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608576"> GRHL2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608576"> 608576 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/52?start=-3&limit=10&highlight=52"> 9p22-p21 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> Deafness, autosomal dominant 47 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> 608652 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> DFNA47 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> 608652 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/216?start=-3&limit=10&highlight=216"> 9q21.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> Deafness, autosomal dominant 51 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="4 - A contiguous gene duplication or deletion syndrome in which multiple genes are involved"> 4 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> 613558 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> DFNA51 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> 613558 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/243?start=-3&limit=10&highlight=243"> 9q21.13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606705"> Deafness, autosomal dominant 36 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606705"> 606705 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606706"> TMC1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606706"> 606706 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/448?start=-3&limit=10&highlight=448"> 9q33.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615629"> Deafness, autosomal dominant 56 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615629"> 615629 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/187380"> TNC </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/187380"> 187380 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/10/112?start=-3&limit=10&highlight=112"> 10p12.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620722"> Deafness, autosomal dominant 90 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620722"> 620722 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606808"> MYO3A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606808"> 606808 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/250?start=-3&limit=10&highlight=250"> 11p14.2-q12.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> Deafness, autosomal dominant 59 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> 612642 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> DFNA59 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> 612642 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/775?start=-3&limit=10&highlight=775"> 11q13.5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601317"> Deafness, autosomal dominant 11 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601317"> 601317 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/276903"> MYO7A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/276903"> 276903 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/1026?start=-3&limit=10&highlight=1026"> 11q23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601543"> Deafness, autosomal dominant 8/12 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601543"> 601543 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602574"> TECTA </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602574"> 602574 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/309?start=-3&limit=10&highlight=309"> 12q13-q14 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> Deafness, autosomal dominant 48 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> 607841 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> DFNA48 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> 607841 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/650?start=-3&limit=10&highlight=650"> 12q21.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617663"> Deafness, autosomal dominant 73 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617663"> 617663 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603317"> PTPRQ </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603317"> 603317 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/666?start=-3&limit=10&highlight=666"> 12q21.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616697"> Deafness, autosomal dominant 69, unilateral or asymmetric </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616697"> 616697 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/184745"> KITLG </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/184745"> 184745 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/719?start=-3&limit=10&highlight=719"> 12q23.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605583"> Deafness, autosomal dominant 25 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605583"> 605583 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607557"> SLC17A8 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607557"> 607557 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/906?start=-3&limit=10&highlight=906"> 12q24.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614152"> Deafness, autosomal dominant 64 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614152"> 614152 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605219"> DIABLO </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605219"> 605219 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/964?start=-3&limit=10&highlight=964"> 12q24.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608224"> Deafness, autosomal dominant 41 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608224"> 608224 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600844"> P2RX2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600844"> 600844 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/13/15?start=-3&limit=10&highlight=15"> 13q12.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601544"> Deafness, autosomal dominant 3A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601544"> 601544 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/121011"> GJB2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/121011"> 121011 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/13/16?start=-3&limit=10&highlight=16"> 13q12.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612643"> Deafness, autosomal dominant 3B </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612643"> 612643 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604418"> GJB6 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604418"> 604418 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/13/319?start=-3&limit=10&highlight=319"> 13q34 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619810"> Deafness, autosomal dominant 84 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619810"> 619810 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605868"> ATP11A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605868"> 605868 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/6?start=-3&limit=10&highlight=6"> 14q11.2-q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> Deafness, autosomal dominant 53 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> 609965 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> DFNA53 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> 609965 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/149?start=-3&limit=10&highlight=149"> 14q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601369"> Deafness, autosomal dominant 9 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601369"> 601369 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603196"> COCH </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603196"> 603196 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/287?start=-3&limit=10&highlight=287"> 14q23.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605192"> Deafness, autosomal dominant 23 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605192"> 605192 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601205"> SIX1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601205"> 601205 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/214?start=-3&limit=10&highlight=214"> 15q21.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617605"> ?Deafness, autosomal dominant 71 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617605"> 617605 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612186"> DMXL2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612186"> 612186 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/419?start=-3&limit=10&highlight=419"> 15q25-q26 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> Deafness, autosomal dominant 30 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> 606451 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> DFNA30 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> 606451 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/458?start=-3&limit=10&highlight=458"> 15q25.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616707"> ?Deafness, autosomal dominant 68 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616707"> 616707 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604799"> HOMER2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604799"> 604799 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/108?start=-3&limit=10&highlight=108"> 16p13.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616044"> Deafness, autosomal dominant 65 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616044"> 616044 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613577"> TBC1D24 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613577"> 613577 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/222?start=-3&limit=10&highlight=222"> 16p13.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618915"> ?Deafness, autosomal dominant 77 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618915"> 618915 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/158343"> ABCC1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/158343"> 158343 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/259?start=-3&limit=10&highlight=259"> 16p12.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616357"> Deafness, autosomal dominant 40 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616357"> 616357 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/123740"> CRYM </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/123740"> 123740 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/1031?start=-3&limit=10&highlight=1031"> 17q25.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604717"> Deafness, autosomal dominant 20/26 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604717"> 604717 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/102560"> ACTG1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/102560"> 102560 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/18/14?start=-3&limit=10&highlight=14"> 18p11.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620280"> ?Deafness, autosomal dominant 86 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620280"> 620280 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606930"> THOC1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606930"> 606930 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/18/80?start=-3&limit=10&highlight=80"> 18q11.1-q11.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619274"> Deafness, autosomal dominant 80 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619274"> 619274 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617782"> GREB1L </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617782"> 617782 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/19/797?start=-3&limit=10&highlight=797"> 19q13.31-q13.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614614"> Deafness, autosomal dominant 4B </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614614"> 614614 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614591"> CEACAM16 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614591"> 614591 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/19/977?start=-3&limit=10&highlight=977"> 19q13.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600652"> Deafness, autosomal dominant 4A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600652"> 600652 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608568"> MYH14 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608568"> 608568 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/20/445?start=-3&limit=10&highlight=445"> 20q13.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616340"> Deafness, autosomal dominant 67 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616340"> 616340 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606731"> OSBPL2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606731"> 606731 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/22/222?start=-3&limit=10&highlight=222"> 22q12.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603622"> Deafness, autosomal dominant 17 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603622"> 603622 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/160775"> MYH9 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/160775"> 160775 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
Not Mapped
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> Deafness, autosomal dominant 33 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> 614211 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> DFNA33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> 614211 </a>
</span>
</td>
</tr>
</tbody>
</table>
</div>
<div class="text-right small">
<a href="#mimPhenotypicSeriesFold" data-toggle="collapse">&#9650;&nbsp;Close</a>
</div>
</div>
</div>
</div>
<div>
<br />
</div>
<div>
<a id="text" class="mim-anchor"></a>
<h4>
<span class="mim-font">
<span class="mim-tip-floating" qtip_title="<strong>Looking For More References?</strong>" qtip_text="Click the 'reference plus' icon &lt;span class='glyphicon glyphicon-plus-sign'&gt;&lt;/span&gt at the end of each OMIM text paragraph to see more references related to the content of the preceding paragraph.">
<strong>TEXT</strong>
</span>
</span>
</h4>
<div>
<a id="clinicalFeatures" class="mim-anchor"></a>
<h4 href="#mimClinicalFeaturesFold" id="mimClinicalFeaturesToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
<span id="mimClinicalFeaturesToggleTriangle" class="small mimTextToggleTriangle">&#9660;</span>
<span class="mim-font">
<strong>Clinical Features</strong>
</span>
</h4>
</div>
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<p><a href="#1" class="mim-tip-reference" title="D&#x27;Adamo, P., Donaudy, F., D&#x27;Eustacchio, A., Di Iorio, E., Melchionda, S., Gasparini, P. &lt;strong&gt;A new locus (DFNA47) for autosomal dominant non-syndromic inherited hearing loss maps to 9p21-22 in a large Italian family.&lt;/strong&gt; Europ. J. Hum. Genet. 11: 121-124, 2003.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/12634859/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;12634859&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1038/sj.ejhg.5200929&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="12634859">D'Adamo et al. (2003)</a> reported a large, multigenerational southern Italian family with an autosomal dominant form of progressive postlingual sensorineural deafness. The hearing loss appeared to be caused by a completely penetrant mutation with a variable age of onset: age 30 to 35 years for the first symptoms, and age 20 to 25 years for the first audiometric abnormalities. An initial high frequency hearing loss progressed with age to include middle and lower frequencies, with a moderate to severe sensorineural deafness invariably present by about age 50. No vestibular dysfunction or other associated abnormalities were noted. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=12634859" 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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<strong>Mapping</strong>
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<p>In a large Italian family with progressive postlingual sensorineural deafness, <a href="#1" class="mim-tip-reference" title="D&#x27;Adamo, P., Donaudy, F., D&#x27;Eustacchio, A., Di Iorio, E., Melchionda, S., Gasparini, P. &lt;strong&gt;A new locus (DFNA47) for autosomal dominant non-syndromic inherited hearing loss maps to 9p21-22 in a large Italian family.&lt;/strong&gt; Europ. J. Hum. Genet. 11: 121-124, 2003.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/12634859/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;12634859&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1038/sj.ejhg.5200929&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="12634859">D'Adamo et al. (2003)</a> identified linkage with a locus, designated DFNA47, on chromosome 9p22-p21 (maximum lod score of 3.67 at theta = 0.0 with D9S162). Using recombinants, they narrowed the candidate region to an approximately 9-cM region between D9S268 and D9S942. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=12634859" 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="#2" class="mim-tip-reference" title="Shahin, H., Walsh, T., Rayyan, A. A., Lee, M. K., Higgins, J., Dickel, D., Lewis, K., Thompson, J., Baker, C., Nord, A. S., Stray, S., Gurwitz, D., Avraham, K. B., King, M.-C., Kanaan, M. &lt;strong&gt;Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.&lt;/strong&gt; Europ. J. Hum. Genet. 18: 407-413, 2010.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/19888295/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;19888295&lt;/a&gt;, &lt;a href=&quot;https://www.ncbi.nlm.nih.gov/pmc/?term=19888295[PMID]&amp;report=imagesdocsum&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed Image&#x27;, &#x27;domain&#x27;: &#x27;ncbi.nlm.nih.gov&#x27;})&quot;&gt;images&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1038/ejhg.2009.190&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="19888295">Shahin et al. (2010)</a> noted that the DFNA47 locus maps within the region of the DFNB83 locus (<a href="/entry/613685">613685</a>) and suggested that mutations in the same gene may be responsible for both the recessive and dominant hearing loss. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=19888295" 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 id="references"class="mim-anchor"></a>
<h4 href="#mimReferencesFold" id="mimReferencesToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
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<strong>REFERENCES</strong>
</span>
</h4>
<div>
<p />
</div>
<div id="mimReferencesFold" class="collapse in mimTextToggleFold">
<ol>
<li>
<a id="1" class="mim-anchor"></a>
<a id="D&#x27;Adamo2003" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
D'Adamo, P., Donaudy, F., D'Eustacchio, A., Di Iorio, E., Melchionda, S., Gasparini, P.
<strong>A new locus (DFNA47) for autosomal dominant non-syndromic inherited hearing loss maps to 9p21-22 in a large Italian family.</strong>
Europ. J. Hum. Genet. 11: 121-124, 2003.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/12634859/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">12634859</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=12634859" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1038/sj.ejhg.5200929" target="_blank">Full Text</a>]
</p>
</div>
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<li>
<a id="2" class="mim-anchor"></a>
<a id="Shahin2010" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Shahin, H., Walsh, T., Rayyan, A. A., Lee, M. K., Higgins, J., Dickel, D., Lewis, K., Thompson, J., Baker, C., Nord, A. S., Stray, S., Gurwitz, D., Avraham, K. B., King, M.-C., Kanaan, M.
<strong>Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.</strong>
Europ. J. Hum. Genet. 18: 407-413, 2010.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/19888295/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">19888295</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/?term=19888295[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=19888295" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1038/ejhg.2009.190" target="_blank">Full Text</a>]
</p>
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<a id="contributors" class="mim-anchor"></a>
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Contributors:
</span>
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<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
Cassandra L. Kniffin - updated : 4/30/2010
</span>
</div>
</div>
</div>
<div>
<a id="creationDate" class="mim-anchor"></a>
<div class="row">
<div class="col-lg-2 col-md-2 col-sm-4 col-xs-4">
<span class="text-nowrap mim-text-font">
Creation Date:
</span>
</div>
<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
Marla J. F. O&#x27;Neill : 5/13/2004
</span>
</div>
</div>
</div>
<div>
<a id="editHistory" class="mim-anchor"></a>
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<div class="col-lg-2 col-md-2 col-sm-4 col-xs-4">
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<a href="#mimCollapseEditHistory" role="button" data-toggle="collapse"> Edit History: </a>
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<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
carol : 01/07/2011
</span>
</div>
</div>
<div class="row collapse" id="mimCollapseEditHistory">
<div class="col-lg-offset-2 col-md-offset-2 col-sm-offset-4 col-xs-offset-4 col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
wwang : 4/30/2010<br>ckniffin : 4/30/2010<br>terry : 12/2/2008<br>carol : 5/21/2004
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<div>
<h3>
<span class="mim-font">
<strong>%</strong> 608652
</span>
</h3>
</div>
<div>
<h3>
<span class="mim-font">
DEAFNESS, AUTOSOMAL DOMINANT 47; DFNA47
</span>
</h3>
</div>
<div>
<br />
</div>
</div>
<div>
<p>
<span class="mim-text-font">
<strong>ORPHA:</strong> 90635; &nbsp;
<strong>DO:</strong> 0110570; &nbsp;
</span>
</p>
</div>
<div>
<br />
</div>
<div>
<p>
<span class="mim-text-font">
<strong>
<em>
Cytogenetic location: 9p22-p21
&nbsp;
Genomic coordinates <span class="small">(GRCh38)</span> : 9:14,200,001-33,200,000 </span>
</em>
</strong>
</span>
</p>
</div>
<div>
<br />
</div>
<div>
<h4>
<span class="mim-font">
<strong>Gene-Phenotype Relationships</strong>
</span>
</h4>
<div>
<table class="table table-bordered table-condensed small mim-table-padding">
<thead>
<tr class="active">
<th>
Location
</th>
<th>
Phenotype
</th>
<th>
Phenotype <br /> MIM number
</th>
<th>
Inheritance
</th>
<th>
Phenotype <br /> mapping key
</th>
</tr>
</thead>
<tbody>
<tr>
<td rowspan="1">
<span class="mim-font">
9p22-p21
</span>
</td>
<td>
<span class="mim-font">
Deafness, autosomal dominant 47
</span>
</td>
<td>
<span class="mim-font">
608652
</span>
</td>
<td>
<span class="mim-font">
Autosomal dominant
</span>
</td>
<td>
<span class="mim-font">
2
</span>
</td>
</tr>
</tbody>
</table>
</div>
</div>
<div>
<br />
</div>
<div>
<h4>
<span class="mim-font">
<strong>TEXT</strong>
</span>
</h4>
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<h4>
<span class="mim-font">
<strong>Clinical Features</strong>
</span>
</h4>
</div>
<span class="mim-text-font">
<p>D'Adamo et al. (2003) reported a large, multigenerational southern Italian family with an autosomal dominant form of progressive postlingual sensorineural deafness. The hearing loss appeared to be caused by a completely penetrant mutation with a variable age of onset: age 30 to 35 years for the first symptoms, and age 20 to 25 years for the first audiometric abnormalities. An initial high frequency hearing loss progressed with age to include middle and lower frequencies, with a moderate to severe sensorineural deafness invariably present by about age 50. No vestibular dysfunction or other associated abnormalities were noted. </p>
</span>
<div>
<br />
</div>
<div>
<h4>
<span class="mim-font">
<strong>Mapping</strong>
</span>
</h4>
</div>
<span class="mim-text-font">
<p>In a large Italian family with progressive postlingual sensorineural deafness, D'Adamo et al. (2003) identified linkage with a locus, designated DFNA47, on chromosome 9p22-p21 (maximum lod score of 3.67 at theta = 0.0 with D9S162). Using recombinants, they narrowed the candidate region to an approximately 9-cM region between D9S268 and D9S942. </p><p>Shahin et al. (2010) noted that the DFNA47 locus maps within the region of the DFNB83 locus (613685) and suggested that mutations in the same gene may be responsible for both the recessive and dominant hearing loss. </p>
</span>
<div>
<br />
</div>
</div>
<div>
<h4>
<span class="mim-font">
<strong>REFERENCES</strong>
</span>
</h4>
<div>
<p />
</div>
<div>
<ol>
<li>
<p class="mim-text-font">
D'Adamo, P., Donaudy, F., D'Eustacchio, A., Di Iorio, E., Melchionda, S., Gasparini, P.
<strong>A new locus (DFNA47) for autosomal dominant non-syndromic inherited hearing loss maps to 9p21-22 in a large Italian family.</strong>
Europ. J. Hum. Genet. 11: 121-124, 2003.
[PubMed: 12634859]
[Full Text: https://doi.org/10.1038/sj.ejhg.5200929]
</p>
</li>
<li>
<p class="mim-text-font">
Shahin, H., Walsh, T., Rayyan, A. A., Lee, M. K., Higgins, J., Dickel, D., Lewis, K., Thompson, J., Baker, C., Nord, A. S., Stray, S., Gurwitz, D., Avraham, K. B., King, M.-C., Kanaan, M.
<strong>Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.</strong>
Europ. J. Hum. Genet. 18: 407-413, 2010.
[PubMed: 19888295]
[Full Text: https://doi.org/10.1038/ejhg.2009.190]
</p>
</li>
</ol>
<div>
<br />
</div>
</div>
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<div class="col-lg-1 col-md-1 col-sm-2 col-xs-2">
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Contributors:
</span>
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<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
Cassandra L. Kniffin - updated : 4/30/2010
</span>
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<br />
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<div class="col-lg-1 col-md-1 col-sm-2 col-xs-2">
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Creation Date:
</span>
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<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
Marla J. F. O&#x27;Neill : 5/13/2004
</span>
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</div>
<div>
<br />
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Edit History:
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carol : 01/07/2011<br>wwang : 4/30/2010<br>ckniffin : 4/30/2010<br>terry : 12/2/2008<br>carol : 5/21/2004
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