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Entry
- %608264 - DEAFNESS, AUTOSOMAL RECESSIVE 40; DFNB40
- OMIM
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<span class="h4">%608264</span>
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<a href="/phenotypicSeries/PS220290"> <strong>Phenotypic Series</strong> </a>
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<div><a href="http://biogps.org/#goto=genereport&id=379003" 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+379003" 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/379003" 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 id="mimClinicalResourcesLinksToggleTriangle" class="small mimSingletonTriangle" style="color: #337CB5; display: table-cell;">&#9660;</div>
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<div style="display: table-cell;">Clinical Resources</div>
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<div><a href="https://clinicaltrials.gov/search?cond=DEAFNESS, AUTOSOMAL RECESSIVE" 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=12047&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=90636" 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> 90636<br />
<strong>DO:</strong> 0110499<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>
608264
</span>
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<div>
<a id="preferredTitle" class="mim-anchor"></a>
<h3>
<span class="mim-font">
DEAFNESS, AUTOSOMAL RECESSIVE 40; DFNB40
</span>
</h3>
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<div>
<br />
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<a id="cytogeneticLocation" class="mim-anchor"></a>
<p>
<span class="mim-text-font">
<strong>
<em>
Cytogenetic location: <a href="/geneMap/22/15?start=-3&limit=10&highlight=15">22q11.21-q12.1</a>
&nbsp;
Genomic coordinates <span class="small">(GRCh38)</span> : <a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&position=chr22:17400001-29200000&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'})">22:17,400,001-29,200,000</a> </span>
</em>
</strong>
</span>
</p>
</div>
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<br />
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<a id="geneMap" class="mim-anchor"></a>
<div style="margin-bottom: 10px;">
<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/22/15?start=-3&limit=10&highlight=15">
22q11.21-q12.1
</a>
</span>
</td>
<td>
<span class="mim-font">
Deafness, autosomal recessive 40
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608264"> 608264 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/608264" class="btn btn-warning" role="button"> Clinical Synopsis </a>
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PheneGene Graphics <span class="caret"></span>
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<li><a href="/graph/linear/608264" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Linear'})"> Linear </a></li>
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</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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<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>
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<div style="margin-left: 2em;">
<div>
<span class="mim-font">
- Autosomal recessive <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/258211005" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">258211005</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0441748&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0441748</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000007" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000007</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000007" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000007</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">
- Deafness, sensorineural, prelingual, profound <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1842343&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1842343</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000399" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000399</a>]</span><br /> -
Hearing threshold at or above 90 dB at all frequencies tested (0.25-8.0 kHz) <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C1842346&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1842346</a>]</span><br />
</span>
</div>
</div>
</div>
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<div class="text-right">
<a href="#mimClinicalSynopsisFold" data-toggle="collapse">&#9650;&nbsp;Close</a>
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<div class="col-lg-12 col-md-12 col-sm-12 col-xs-12">
<h5>
Deafness, autosomal recessive
- <a href="/phenotypicSeries/PS220290">PS220290</a>
- 109 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/1/87?start=-3&limit=10&highlight=87"> 1p36.31-p36.13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614414"> Deafness, autosomal recessive 96 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/614414"> 614414 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614414"> DFNB96 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614414"> 614414 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/98?start=-3&limit=10&highlight=98"> 1p36.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609006"> Deafness, autosomal recessive 36 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/609006"> 609006 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606351"> ESPN </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606351"> 606351 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/98?start=-3&limit=10&highlight=98"> 1p36.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609006"> Deafness, neurosensory, without vestibular involvement, autosomal dominant </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/609006"> 609006 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606351"> ESPN </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606351"> 606351 </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/220290"> Deafness, digenic, GJB2/GJB3 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</abbr>, <abbr class="mim-tip-hint" title="Digenic dominant">DD</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/220290"> 220290 </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/1/682?start=-3&limit=10&highlight=682"> 1p31.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617654"> ?Deafness, autosomal recessive 108 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/617654"> 617654 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602336"> ROR1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602336"> 602336 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/838?start=-3&limit=10&highlight=838"> 1p21.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608653"> Deafness, autosomal recessive 32, with or without immotile sperm </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/608653"> 608653 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603504"> CDC14A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603504"> 603504 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1307?start=-3&limit=10&highlight=1307"> 1q23.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600791"> Enlarged vestibular aqueduct, digenic </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/600791"> 600791 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602208"> KCNJ10 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602208"> 602208 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1825?start=-3&limit=10&highlight=1825"> 1q43-q44 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612433"> Deafness, autosomal recessive 45 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/612433"> 612433 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612433"> DFNB45 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612433"> 612433 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/26?start=-3&limit=10&highlight=26"> 2p25.1-p24.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609946"> Deafness, neurosensory, autosomal recessive 47 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/609946"> 609946 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609946"> DFNB47 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609946"> 609946 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/108?start=-3&limit=10&highlight=108"> 2p23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601071"> Deafness, autosomal recessive 9 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/601071"> 601071 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603681"> OTOF </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603681"> 603681 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/108?start=-3&limit=10&highlight=108"> 2p23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601071"> Auditory neuropathy, autosomal recessive, 1 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/601071"> 601071 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603681"> OTOF </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603681"> 603681 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/269?start=-3&limit=10&highlight=269"> 2p16.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614934"> Deafness, autosomal recessive 70, with or without adult-onset neurodegeneration </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/614934"> 614934 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610316"> PNPT1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610316"> 610316 </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/615429"> ?Deafness, autosomal recessive 88 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/615429"> 615429 </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/2/676?start=-3&limit=10&highlight=676"> 2q23-q31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605818"> Deafness, autosomal recessive 27 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/605818"> 605818 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605818"> DFNB27 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605818"> 605818 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/820?start=-3&limit=10&highlight=820"> 2q31.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610220"> Deafness, autosomal recessive 59 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/610220"> 610220 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610219"> PJVK </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610219"> 610219 </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/601386"> {Deafness, autosomal recessive 12, modifier of} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/601386"> 601386 </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/3/257?start=-3&limit=10&highlight=257"> 3p21.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600971"> Deafness, autosomal recessive 6 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/600971"> 600971 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607237"> TMIE </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607237"> 607237 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/582?start=-3&limit=10&highlight=582"> 3q13.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620551"> Deafness, autosomal recessive 121 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/620551"> 620551 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610464"> GPR156 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610464"> 610464 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/597?start=-3&limit=10&highlight=597"> 3q13.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609646"> Deafness, autosomal recessive 42 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/609646"> 609646 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609739"> ILDR1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609739"> 609739 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/116?start=-3&limit=10&highlight=116"> 4p15.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619174"> Deafness, autosomal recessive 117 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/619174"> 619174 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618988"> CLRN2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618988"> 618988 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/181?start=-3&limit=10&highlight=181"> 4p13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613285"> Deafness, autosomal recessive 25 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/613285"> 613285 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613283"> GRXCR1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613283"> 613283 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/209?start=-3&limit=10&highlight=209"> 4q12-q13.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609952"> Deafness, autosomal recessive 55 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/609952"> 609952 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609952"> DFNB55 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609952"> 609952 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/578?start=-3&limit=10&highlight=578"> 4q31.21 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605428"> ?Deafness, autosomal recessive 26 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/605428"> 605428 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604439"> GAB1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604439"> 604439 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/228?start=-3&limit=10&highlight=228"> 5q13.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610153"> Deafness, autosomal recessive 49 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/610153"> 610153 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610572"> MARVELD2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610572"> 610572 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/236?start=-3&limit=10&highlight=236"> 5q13.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618257"> ?Deafness, autosomal recessive 112 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/618257"> 618257 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607012"> BDP1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607012"> 607012 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/349?start=-3&limit=10&highlight=349"> 5q21.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618422"> Deafness, autosomal recessive 100 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/618422"> 618422 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611648"> PPIP5K2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611648"> 611648 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/417?start=-3&limit=10&highlight=417"> 5q23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620238"> Deafness, autosomal recessive 120 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/620238"> 620238 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620215"> MINAR2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620215"> 620215 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/626?start=-3&limit=10&highlight=626"> 5q32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615837"> ?Deafness, autosomal recessive 101 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/615837"> 615837 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615762"> GRXCR2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615762"> 615762 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/751?start=-3&limit=10&highlight=751"> 5q35.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600791"> Enlarged vestibular aqueduct </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/600791"> 600791 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601093"> FOXI1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601093"> 601093 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/18?start=-3&limit=10&highlight=18"> 6p25.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613453"> ?Deafness, autosomal recessive 91 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/613453"> 613453 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/173321"> SERPINB6 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/173321"> 173321 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/110?start=-3&limit=10&highlight=110"> 6p22.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610212"> ?Deafness, autosomal recessive 66 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/610212"> 610212 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605755"> DCDC2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605755"> 605755 </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/616515"> ?Deafness, autosomal recessive 104 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/616515"> 616515 </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/6/383?start=-3&limit=10&highlight=383"> 6p21.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609706"> Deafness, autosomal recessive 53 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/609706"> 609706 </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/6/434?start=-3&limit=10&highlight=434"> 6p21.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610265"> Deafness, autosomal recessive 67 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/610265"> 610265 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609427"> LHFPL5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609427"> 609427 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/549?start=-3&limit=10&highlight=549"> 6p21.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616042"> ?Deafness, autosomal recessive 103 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/616042"> 616042 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607293"> CLIC5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607293"> 607293 </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/607821"> Deafness, autosomal recessive 37 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/607821"> 607821 </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/6/1006?start=-3&limit=10&highlight=1006"> 6q26-q27 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608219"> Deafness, autosomal recessive 38 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/608219"> 608219 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608219"> DFNB38 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608219"> 608219 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/249?start=-3&limit=10&highlight=249"> 7p12.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610154"> ?Deafness, autosomal recessive 44 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/610154"> 610154 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/103072"> ADCY1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/103072"> 103072 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/376?start=-3&limit=10&highlight=376"> 7q21.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608265"> Deafness, autosomal recessive 39 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/608265"> 608265 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/142409"> HGF </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/142409"> 142409 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/558?start=-3&limit=10&highlight=558"> 7q22.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613865"> ?Deafness, autosomal recessive 61 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/613865"> 613865 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604943"> SLC26A5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604943"> 604943 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/577?start=-3&limit=10&highlight=577"> 7q22.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600791"> Deafness, autosomal recessive 4, with enlarged vestibular aqueduct </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/600791"> 600791 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605646"> SLC26A4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605646"> 605646 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/581?start=-3&limit=10&highlight=581"> 7q31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603678"> Deafness, autosomal recessive 14 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/603678"> 603678 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603678"> DFNB14 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603678"> 603678 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/582?start=-3&limit=10&highlight=582"> 7q31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603010"> Deafness, autosomal recessive 17 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/603010"> 603010 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603010"> DFNB17 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603010"> 603010 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/604?start=-3&limit=10&highlight=604"> 7q31.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616705"> ?Deafness, autosomal recessive 97 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/616705"> 616705 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/164860"> MET </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/164860"> 164860 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/721?start=-3&limit=10&highlight=721"> 7q34-q36 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603098"> Deafness, autosomal recessive 13 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/603098"> 603098 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603098"> DFNB13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603098"> 603098 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/8/66?start=-3&limit=10&highlight=66"> 8p22-p21.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612789"> Deafness, autosomal recessive 71 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/612789"> 612789 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612789"> DFNB71 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612789"> 612789 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/8/400?start=-3&limit=10&highlight=400"> 8q22 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619553"> Deafness, autosomal recessive 118, with cochlear aplasia </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/619553"> 619553 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619553"> DFNB118 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619553"> 619553 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/8/412?start=-3&limit=10&highlight=412"> 8q22.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618013"> ?Deafness, autosomal recessive 109 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/618013"> 618013 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612959"> ESRP1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612959"> 612959 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/8/484?start=-3&limit=10&highlight=484"> 8q23.1-q23.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620794"> Deafness, autosomal recessive 124 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/620794"> 620794 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607843"> PKHD1L1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607843"> 607843 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/45?start=-3&limit=10&highlight=45"> 9p23-p21.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613685"> Deafness, autosomal recessive 83 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/613685"> 613685 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613685"> DFNB83 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613685"> 613685 </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/600974"> Deafness, autosomal recessive 7 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/600974"> 600974 </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/9/443?start=-3&limit=10&highlight=443"> 9q32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607084"> Deafness, autosomal recessive 31 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/607084"> 607084 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607928"> WHRN </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607928"> 607928 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/687?start=-3&limit=10&highlight=687"> 9q34.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613307"> Deafness, autosomal recessive 79 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/613307"> 613307 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613354"> TPRN </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613354"> 613354 </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/607101"> Deafness, autosomal recessive 30 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/607101"> 607101 </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/10/128?start=-3&limit=10&highlight=128"> 10p11.23-q21.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607239"> Deafness, autosomal recessive 33 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/607239"> 607239 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607239"> DFNB33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607239"> 607239 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/10/209?start=-3&limit=10&highlight=209"> 10q21.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609533"> Deafness, autosomal recessive 23 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/609533"> 609533 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605514"> PCDH15 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605514"> 605514 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/10/281?start=-3&limit=10&highlight=281"> 10q22.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601386"> Deafness, autosomal recessive 12 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/601386"> 601386 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605516"> CDH23 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605516"> 605516 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/10/491?start=-3&limit=10&highlight=491"> 10q24.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618003"> Deafness, autosomal recessive 57 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/618003"> 618003 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612971"> PDZD7 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612971"> 612971 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/39?start=-3&limit=10&highlight=39"> 11p15.5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617637"> Deafness autosomal recessive 106 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/617637"> 617637 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614988"> EPS8L2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614988"> 614988 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/210?start=-3&limit=10&highlight=210"> 11p15.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602092"> Deafness, autosomal recessive 18A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/602092"> 602092 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605242"> USH1C </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605242"> 605242 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/211?start=-3&limit=10&highlight=211"> 11p15.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614945"> Deafness, autosomal recessive 18B </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/614945"> 614945 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604487"> OTOG </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604487"> 604487 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/246?start=-3&limit=10&highlight=246"> 11p14.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620877"> ?Deafness, autosomal recessive 125 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/620877"> 620877 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602835"> GAS2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602835"> 602835 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/273?start=-3&limit=10&highlight=273"> 11p13-p12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609941"> Deafness, autosomal recessive 51 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/609941"> 609941 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609941"> DFNB51 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609941"> 609941 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/670?start=-3&limit=10&highlight=670"> 11q13.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614899"> Deafness, autosomal recessive 93 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/614899"> 614899 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607314"> CABP2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607314"> 607314 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/714?start=-3&limit=10&highlight=714"> 11q13.4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611451"> Deafness, autosomal recessive 63 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/611451"> 611451 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612414"> LRTOMT </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612414"> 612414 </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/600060"> Deafness, autosomal recessive 2 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/600060"> 600060 </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/11/792?start=-3&limit=10&highlight=792"> 11q14.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618434"> ?Deafness, autosomal recessive 94 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/618434"> 618434 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612803"> NARS2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612803"> 612803 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/902?start=-3&limit=10&highlight=902"> 11q22.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611022"> Deafness, autosomal recessive 24 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/611022"> 611022 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/179410"> RDX </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/179410"> 179410 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/980?start=-3&limit=10&highlight=980"> 11q23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618145"> Deafness, autosomal recessive 111 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/618145"> 618145 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604873"> MPZL2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604873"> 604873 </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/603629"> Deafness, autosomal recessive 21 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/603629"> 603629 </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/11/1096?start=-3&limit=10&highlight=1096"> 11q25-qter </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604060"> Deafness, autosomal recessive 20 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/604060"> 604060 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604060"> DFNB20 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604060"> 604060 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/133?start=-3&limit=10&highlight=133"> 12p13.2-p11.23 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610143"> Deafness, autosomal recessive 62 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/610143"> 610143 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610143"> DFNB62 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610143"> 610143 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/203?start=-3&limit=10&highlight=203"> 12p12.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615974"> ?Deafness, autosomal recessive 102 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/615974"> 615974 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600206"> EPS8 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600206"> 600206 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/588?start=-3&limit=10&highlight=588"> 12q14.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613718"> Deafness, autosomal recessive 74 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/613718"> 613718 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613719"> MSRB3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613719"> 613719 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/649?start=-3&limit=10&highlight=649"> 12q21.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614944"> Deafness, autosomal recessive 84B </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/614944"> 614944 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614925"> OTOGL </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614925"> 614925 </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/613391"> Deafness, autosomal recessive 84A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/613391"> 613391 </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/13/15?start=-3&limit=10&highlight=15"> 13q12.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/220290"> Deafness, autosomal recessive 1A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</abbr>, <abbr class="mim-tip-hint" title="Digenic dominant">DD</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/220290"> 220290 </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/612645"> Deafness, autosomal recessive 1B </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/612645"> 612645 </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/13/16?start=-3&limit=10&highlight=16"> 13q12.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/220290"> Deafness, digenic GJB2/GJB6 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</abbr>, <abbr class="mim-tip-hint" title="Digenic dominant">DD</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/220290"> 220290 </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/13/288?start=-3&limit=10&highlight=288"> 13q32.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620714"> ?Deafness, autosomal recessive 122 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/620714"> 620714 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618203"> TMTC4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618203"> 618203 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/110?start=-3&limit=10&highlight=110"> 14q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600792"> Deafness, autosomal recessive 5 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/600792"> 600792 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600792"> DFNB5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600792"> 600792 </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/618094"> ?Deafness, autosomal recessive 110 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/618094"> 618094 </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/14/407?start=-3&limit=10&highlight=407"> 14q24.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608565"> Deafness, autosomal recessive 35 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/608565"> 608565 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602167"> ESRRB </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602167"> 602167 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/154?start=-3&limit=10&highlight=154"> 15q15.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603720"> Deafness, autosomal recessive 16 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/603720"> 603720 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606440"> STRC </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606440"> 606440 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/181?start=-3&limit=10&highlight=181"> 15q21.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619615"> Deafness, autosomal recessive 119 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/619615"> 619615 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619578"> AFG2B </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619578"> 619578 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/421?start=-3&limit=10&highlight=421"> 15q25.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609439"> Deafness, autosomal recessive 48 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/609439"> 609439 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605564"> CIB2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605564"> 605564 </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/614617"> Deafness, autosomal recessive 86 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/614617"> 614617 </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/16/125?start=-3&limit=10&highlight=125"> 16p13.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619093"> Deafness, autosomal recessive 116 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/619093"> 619093 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615799"> CLDN9 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615799"> 615799 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/263?start=-3&limit=10&highlight=263"> 16p12.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607039"> Deafness, autosomal recessive 22 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/607039"> 607039 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607038"> OTOA </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607038"> 607038 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/375?start=-3&limit=10&highlight=375"> 16p11.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620745"> ?Deafness, autosomal recessive 123 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/620745"> 620745 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/186591"> STX4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/186591"> 186591 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/655?start=-3&limit=10&highlight=655"> 16q23.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613916"> Deafness, autosomal recessive 89 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/613916"> 613916 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601421"> KARS1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601421"> 601421 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/76?start=-3&limit=10&highlight=76"> 17p13.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618457"> ?Deafness, autosomal recessive 115 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/618457"> 618457 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612584"> SPNS2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612584"> 612584 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/230?start=-3&limit=10&highlight=230"> 17p12-q11.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613392"> Deafness, autosomal recessive 85 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/613392"> 613392 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613392"> DFNB85 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613392"> 613392 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/278?start=-3&limit=10&highlight=278"> 17p11.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600316"> Deafness, autosomal recessive 3 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/600316"> 600316 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602666"> MYO15A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602666"> 602666 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/292?start=-3&limit=10&highlight=292"> 17p11.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618456"> Deafness, autosomal recessive 114 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/618456"> 618456 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604330"> GRAP </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604330"> 604330 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/411?start=-3&limit=10&highlight=411"> 17q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618481"> Deafness, autosomal recessive 99 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/618481"> 618481 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616178"> TMEM132E </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616178"> 616178 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/955?start=-3&limit=10&highlight=955"> 17q25.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617639"> Deafness, autosomal recessive 107 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/617639"> 617639 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606962"> WBP2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606962"> 606962 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/18/3?start=-3&limit=10&highlight=3"> 18p11.32-p11.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609647"> Deafness, autosomal recessive 46 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/609647"> 609647 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609647"> DFNB46 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609647"> 609647 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/18/162?start=-3&limit=10&highlight=162"> 18q21.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613079"> Deafness, autosomal recessive 77 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/613079"> 613079 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613072"> LOXHD1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613072"> 613072 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/19/110?start=-3&limit=10&highlight=110"> 19p13.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601869"> Deafness, autosomal recessive 15 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/601869"> 601869 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608792"> GIPC3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608792"> 608792 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/19/261?start=-3&limit=10&highlight=261"> 19p13.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610419"> Deafness, autosomal recessive 68 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/610419"> 610419 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605111"> S1PR2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605111"> 605111 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/19/610?start=-3&limit=10&highlight=610"> 19q13.12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615540"> Deafness, autosomal recessive 76 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/615540"> 615540 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615535"> SYNE4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615535"> 615535 </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/618410"> Deafness, autosomal recessive 113 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/618410"> 618410 </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/20/391?start=-3&limit=10&highlight=391"> 20q13.2-q13.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610248"> Deafness, autosomal recessive 65 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/610248"> 610248 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610248"> DFNB65 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610248"> 610248 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/21/93?start=-3&limit=10&highlight=93"> 21q22.13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614035"> Deafness, autosomal recessive 29 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/614035"> 614035 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605608"> CLDN14 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605608"> 605608 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/21/134?start=-3&limit=10&highlight=134"> 21q22.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601072"> Deafness, autosomal recessive 8/10 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/601072"> 601072 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605511"> TMPRSS3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605511"> 605511 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/21/162?start=-3&limit=10&highlight=162"> 21q22.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614861"> ?Deafness, autosomal recessive 98 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/614861"> 614861 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612920"> TSPEAR </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612920"> 612920 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/22/15?start=-3&limit=10&highlight=15"> 22q11.21-q12.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608264"> Deafness, autosomal recessive 40 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/608264"> 608264 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608264"> DFNB40 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608264"> 608264 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/22/254?start=-3&limit=10&highlight=254"> 22q13.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609823"> Deafness, autosomal recessive 28 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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/609823"> 609823 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609761"> TRIOBP </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609761"> 609761 </a>
</span>
</td>
</tr>
</tbody>
</table>
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<a href="#mimPhenotypicSeriesFold" data-toggle="collapse">&#9650;&nbsp;Close</a>
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<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>
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<span id="mimMappingToggleTriangle" class="small mimTextToggleTriangle">&#9660;</span>
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<strong>Mapping</strong>
</span>
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<span class="mim-text-font">
<p>In a consanguineous Iranian family in which several members had an autosomal recessive form of prelingual profound sensorineural hearing loss, <a href="#1" class="mim-tip-reference" title="Delmaghani, S., Aghaie, A., Compain-Nouaille, S., Ataie, A., Lemainque, A., Zeinali, S., Lathrop, M, Weil, D., Petit, C. &lt;strong&gt;DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.&lt;/strong&gt; Europ. J. Hum. Genet. 11: 816-818, 2003.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/14512974/&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;14512974&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1038/sj.ejhg.5201045&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="14512974">Delmaghani et al. (2003)</a> found linkage of the disorder to a locus, designated DFNB40, on chromosome 22q11.21-q12.1. The approximately 9-Mb interval was bordered by markers D22S427 and D22S1144; a maximum lod score of 3.09 was obtained with D22S1174. The authors noted that the 'Bronx waltzer' (bv) mouse mutant, characterized by waltzing behavior, deafness, and degeneration of cochlear inner hair cells, had been mapped to mouse chromosome 5 in a region of syntenic homology to 22q. They suggested that DFNB40 and bv may result from orthologous gene defects. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=14512974" 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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<h4 href="#mimReferencesFold" id="mimReferencesToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
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<span id="mimReferencesToggleTriangle" class="small mimTextToggleTriangle">&#9660;</span>
<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="Delmaghani2003" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Delmaghani, S., Aghaie, A., Compain-Nouaille, S., Ataie, A., Lemainque, A., Zeinali, S., Lathrop, M, Weil, D., Petit, C.
<strong>DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.</strong>
Europ. J. Hum. Genet. 11: 816-818, 2003.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/14512974/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">14512974</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=14512974" 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.5201045" target="_blank">Full Text</a>]
</p>
</div>
</li>
</ol>
<div>
<br />
</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">
Victor A. McKusick : 11/14/2003
</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">
<span class="text-nowrap mim-text-font">
<a href="#mimCollapseEditHistory" role="button" data-toggle="collapse"> Edit History: </a>
</span>
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<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
carol : 12/02/2008
</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">
carol : 3/18/2004<br>carol : 11/14/2003<br>carol : 11/14/2003
</span>
</div>
</div>
</div>
</div>
</div>
</div>
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<div class="row">
<div class="col-md-8 col-md-offset-1">
<div>
<div>
<h3>
<span class="mim-font">
<strong>%</strong> 608264
</span>
</h3>
</div>
<div>
<h3>
<span class="mim-font">
DEAFNESS, AUTOSOMAL RECESSIVE 40; DFNB40
</span>
</h3>
</div>
<div>
<br />
</div>
</div>
<div>
<p>
<span class="mim-text-font">
<strong>ORPHA:</strong> 90636; &nbsp;
<strong>DO:</strong> 0110499; &nbsp;
</span>
</p>
</div>
<div>
<br />
</div>
<div>
<p>
<span class="mim-text-font">
<strong>
<em>
Cytogenetic location: 22q11.21-q12.1
&nbsp;
Genomic coordinates <span class="small">(GRCh38)</span> : 22:17,400,001-29,200,000 </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">
22q11.21-q12.1
</span>
</td>
<td>
<span class="mim-font">
Deafness, autosomal recessive 40
</span>
</td>
<td>
<span class="mim-font">
608264
</span>
</td>
<td>
<span class="mim-font">
Autosomal recessive
</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>
<div>
<h4>
<span class="mim-font">
<strong>Mapping</strong>
</span>
</h4>
</div>
<span class="mim-text-font">
<p>In a consanguineous Iranian family in which several members had an autosomal recessive form of prelingual profound sensorineural hearing loss, Delmaghani et al. (2003) found linkage of the disorder to a locus, designated DFNB40, on chromosome 22q11.21-q12.1. The approximately 9-Mb interval was bordered by markers D22S427 and D22S1144; a maximum lod score of 3.09 was obtained with D22S1174. The authors noted that the 'Bronx waltzer' (bv) mouse mutant, characterized by waltzing behavior, deafness, and degeneration of cochlear inner hair cells, had been mapped to mouse chromosome 5 in a region of syntenic homology to 22q. They suggested that DFNB40 and bv may result from orthologous gene defects. </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">
Delmaghani, S., Aghaie, A., Compain-Nouaille, S., Ataie, A., Lemainque, A., Zeinali, S., Lathrop, M, Weil, D., Petit, C.
<strong>DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.</strong>
Europ. J. Hum. Genet. 11: 816-818, 2003.
[PubMed: 14512974]
[Full Text: https://doi.org/10.1038/sj.ejhg.5201045]
</p>
</li>
</ol>
<div>
<br />
</div>
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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">
Victor A. McKusick : 11/14/2003
</span>
</div>
</div>
</div>
<div>
<br />
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<div class="col-lg-1 col-md-1 col-sm-2 col-xs-2">
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Edit History:
</span>
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<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
carol : 12/02/2008<br>carol : 3/18/2004<br>carol : 11/14/2003<br>carol : 11/14/2003
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