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1:
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612643.
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DEAFNESS, AUTOSOMAL DOMINANT 3B; DFNA3B
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Cytogenetic location:
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13q12.11</a></span>
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<span class="text-success">Matching terms: <span class="mim-font">612643</span></span>
<br />
<a href="#mimPhenotypeMapFold_1" id="mimPhenotypeMapToggle_1" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'GeneMap'})"><span class="small"><span id="mimPhenotypeMapToggleTriangle_1" class="mimPingletonToggleTriangle" style="color: DarkOrchid">►</span> Phenotype-Gene Relationships</span></a>
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<a href="#mimDisorderCodesFold_1" id="mimDisorderCodesToggle_1" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'ICD+'})"><span class="small"><span id="mimDisorderCodesToggleTriangle_1" class="mimSingletonToggleTriangle" style="color: DarkRed">►</span> ICD+</span></a>
<a href="#mimLinksFold_1" id="mimLinksToggle_1" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'Links'})"><span class="small"><span id="mimLinksToggleTriangle_1" class="mimSingletonToggleTriangle" style="color: #337CB5">►</span> Links</span></a>
<div id="mimPhenotypeMapFold_1" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-bordered table-condensed small mim-table-padding">
<caption>
Phenotype-Gene Relationships
</caption>
<thead>
<tr>
<th>
Location
</th>
<th>
Phenotype
</th>
<th>
Phenotype <br /> MIM number
</th>
<th>
Inheritance
</th>
<th>
Phenotype <br /> mapping key
</th>
<th>
Gene/Locus
</th>
<th>
Gene/Locus <br /> MIM number
</th>
</tr>
</thead>
<tbody>
<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">
Deafness, autosomal dominant 3B
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612643"> 612643 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
GJB6
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604418"> 604418 </a>
</span>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimPhenotypeMapFold_1" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimPhenotypicSeriesFold_1" class="well well-sm collapse mimSingletonToggleFold">
<div class="small">
<div class="row">
<div class="col-lg-12 col-md-12 col-sm-12 col-xs-12">
<h5>
Deafness, autosomal dominant
- <a href="/phenotypicSeries/PS124900">PS124900</a>
- 75 Entries
</h5>
</div>
</div>
<div class="row" style="margin-left: 0.125em; margin-right: 0.125em;">
<table class="table table-bordered table-condensed table-hover mim-table-padding">
<thead>
<tr>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Location</strong>
</th>
<th class="col-lg-5 col-md-5 col-sm-5 col-xs-6 text-nowrap">
<strong>Phenotype</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Inheritance</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Phenotype<br />mapping key</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Phenotype<br />MIM number</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Gene/Locus</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Gene/Locus<br />MIM number</strong>
</th>
</tr>
</thead>
<tbody>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/253?start=-3&limit=10&highlight=253"> 1p36.12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620227"> Deafness, autosomal dominant 85 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620227"> 620227 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617445"> USP48 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617445"> 617445 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/423?start=-3&limit=10&highlight=423"> 1p34.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612644"> Deafness, autosomal dominant 2B, with or without peripheral neuropathy </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612644"> 612644 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603324"> GJB3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603324"> 603324 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/456?start=-3&limit=10&highlight=456"> 1p34.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620283"> ?Deafness, autosomal dominant 88 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620283"> 620283 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611123"> EPHA10 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611123"> 611123 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/495?start=-3&limit=10&highlight=495"> 1p34.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600101"> Deafness, autosomal dominant 2A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600101"> 600101 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603537"> KCNQ4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603537"> 603537 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/847?start=-3&limit=10&highlight=847"> 1p21.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618533"> Deafness, autosomal dominant 37 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618533"> 618533 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120280"> COL11A1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120280"> 120280 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/997?start=-3&limit=10&highlight=997"> 1q21-q23 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> Deafness, autosomal dominant 49 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> 608372 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> DFNA49 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> 608372 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1096?start=-3&limit=10&highlight=1096"> 1q21.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620281"> Deafness, autosomal dominant 87 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620281"> 620281 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602758"> PI4KB </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602758"> 602758 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1373?start=-3&limit=10&highlight=1373"> 1q23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601412"> Deafness, autosomal dominant 7 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601412"> 601412 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600298"> LMX1A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600298"> 600298 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1862?start=-3&limit=10&highlight=1862"> 1q44 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617772"> Deafness, autosomal dominant 34, with or without inflammation </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617772"> 617772 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606416"> NLRP3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606416"> 606416 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/205?start=-3&limit=10&highlight=205"> 2p21-p12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> Deafness, autosomal dominant 58 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="4 - A contiguous gene duplication or deletion syndrome in which multiple genes are involved"> 4 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> 615654 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> DFNA58 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> 615654 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/396?start=-3&limit=10&highlight=396"> 2p12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> Deafness, autosomal dominant 43 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> 608394 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> DFNA43 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> 608394 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/421?start=-3&limit=10&highlight=421"> 2p11.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619500"> ?Deafness, autosomal dominant 81 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619500"> 619500 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615427"> ELMOD3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615427"> 615427 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/675?start=-3&limit=10&highlight=675"> 2q23-q24.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> Deafness, autosomal dominant 16 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> 603964 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> DFNA16 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> 603964 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/58?start=-3&limit=10&highlight=58"> 3p25.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619804"> Deafness, autosomal dominant 82 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619804"> 619804 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/108733"> ATP2B2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/108733"> 108733 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/643?start=-3&limit=10&highlight=643"> 3q21.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616968"> ?Deafness, autosomal dominant 70 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616968"> 616968 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/116945"> MCM2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/116945"> 116945 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/665?start=-3&limit=10&highlight=665"> 3q22 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> Deafness, autosomal dominant 18 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> 606012 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> DFNA18 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> 606012 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/745?start=-3&limit=10&highlight=745"> 3q23 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618787"> Deafness, autosomal dominant 76 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618787"> 618787 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602734"> PLS1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602734"> 602734 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/966?start=-3&limit=10&highlight=966"> 3q28 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607453"> ?Deafness, autosomal dominant 44 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607453"> 607453 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611051"> CCDC50 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611051"> 611051 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/69?start=-3&limit=10&highlight=69"> 4p16.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600965"> Deafness, autosomal dominant 6/14/38 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600965"> 600965 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606201"> WFS1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606201"> 606201 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/243?start=-3&limit=10&highlight=243"> 4q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612431"> Deafness, autosomal dominant 27 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612431"> 612431 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600571"> REST </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600571"> 600571 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/365?start=-3&limit=10&highlight=365"> 4q21.22 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619086"> ?Deafness, autosomal dominant 79 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619086"> 619086 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608370"> SCD5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608370"> 608370 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/415?start=-3&limit=10&highlight=415"> 4q22.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620284"> ?Deafness, autosomal dominant 89 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620284"> 620284 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601461"> ATOH1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601461"> 601461 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/696?start=-3&limit=10&highlight=696"> 4q35-qter </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> Deafness, autosomal dominant 24 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> 606282 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> DFNA24 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> 606282 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/239?start=-3&limit=10&highlight=239"> 5q13.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619808"> ?Deafness, autosomal dominant 83 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619808"> 619808 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/157129"> MAP1B </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/157129"> 157129 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/412?start=-3&limit=10&highlight=412"> 5q23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619081"> Deafness, autosomal dominant 78 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619081"> 619081 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600840"> SLC12A2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600840"> 600840 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/424?start=-3&limit=10&highlight=424"> 5q31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> Deafness, autosomal dominant 54 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> 615649 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> DFNA54 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> 615649 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/605?start=-3&limit=10&highlight=605"> 5q31.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/124900"> Deafness, autosomal dominant 1, with or without thrombocytopenia </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/124900"> 124900 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602121"> DIAPH1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602121"> 602121 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/630?start=-3&limit=10&highlight=630"> 5q32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602459"> Deafness, autosomal dominant 15/52 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602459"> 602459 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602460"> POU4F3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602460"> 602460 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/119?start=-3&limit=10&highlight=119"> 6p22.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607017"> Deafness, autosomal dominant 21 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607017"> 607017 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611410"> RIPOR2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611410"> 611410 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/245?start=-3&limit=10&highlight=245"> 6p21.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> Deafness, autosomal dominant 31 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> 608645 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> DFNA31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> 608645 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/340?start=-3&limit=10&highlight=340"> 6p21.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617606"> ?Deafness, autosomal dominant 72 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617606"> 617606 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606107"> SLC44A4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606107"> 606107 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/383?start=-3&limit=10&highlight=383"> 6p21.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601868"> Deafness, autosomal dominant 13 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601868"> 601868 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120290"> COL11A2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120290"> 120290 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/658?start=-3&limit=10&highlight=658"> 6q14.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> Deafness, autosomal dominant 22 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> 606346 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> MYO6 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> 600970 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/658?start=-3&limit=10&highlight=658"> 6q14.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> 606346 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> MYO6 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> 600970 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/764?start=-3&limit=10&highlight=764"> 6q21 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616969"> ?Deafness, autosomal dominant 66 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616969"> 616969 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603356"> CD164 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603356"> 603356 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/874?start=-3&limit=10&highlight=874"> 6q23.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601316"> Deafness, autosomal dominant 10 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601316"> 601316 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603550"> EYA4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603550"> 603550 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/120?start=-3&limit=10&highlight=120"> 7p15.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600994"> Deafness, autosomal dominant 5 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600994"> 600994 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608798"> GSDME </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608798"> 608798 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/172?start=-3&limit=10&highlight=172"> 7p14.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618140"> ?Deafness, autosomal dominant 74 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618140"> 618140 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602987"> PDE1C </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602987"> 602987 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/457?start=-3&limit=10&highlight=457"> 7q22.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618778"> ?Deafness, autosomal dominant 75 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618778"> 618778 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603015"> TRRAP </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603015"> 603015 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/671?start=-3&limit=10&highlight=671"> 7q32.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613074"> Deafness, autosomal dominant 50 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613074"> 613074 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611606"> MIR96 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611606"> 611606 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/8/450?start=-3&limit=10&highlight=450"> 8q22.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608641"> Deafness, autosomal dominant 28 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608641"> 608641 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608576"> GRHL2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608576"> 608576 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/52?start=-3&limit=10&highlight=52"> 9p22-p21 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> Deafness, autosomal dominant 47 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> 608652 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> DFNA47 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> 608652 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/216?start=-3&limit=10&highlight=216"> 9q21.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> Deafness, autosomal dominant 51 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="4 - A contiguous gene duplication or deletion syndrome in which multiple genes are involved"> 4 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> 613558 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> DFNA51 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> 613558 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/243?start=-3&limit=10&highlight=243"> 9q21.13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606705"> Deafness, autosomal dominant 36 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606705"> 606705 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606706"> TMC1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606706"> 606706 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/448?start=-3&limit=10&highlight=448"> 9q33.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615629"> Deafness, autosomal dominant 56 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615629"> 615629 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/187380"> TNC </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/187380"> 187380 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/10/112?start=-3&limit=10&highlight=112"> 10p12.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620722"> Deafness, autosomal dominant 90 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620722"> 620722 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606808"> MYO3A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606808"> 606808 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/250?start=-3&limit=10&highlight=250"> 11p14.2-q12.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> Deafness, autosomal dominant 59 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> 612642 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> DFNA59 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> 612642 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/775?start=-3&limit=10&highlight=775"> 11q13.5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601317"> Deafness, autosomal dominant 11 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601317"> 601317 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/276903"> MYO7A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/276903"> 276903 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/1026?start=-3&limit=10&highlight=1026"> 11q23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601543"> Deafness, autosomal dominant 8/12 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601543"> 601543 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602574"> TECTA </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602574"> 602574 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/309?start=-3&limit=10&highlight=309"> 12q13-q14 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> Deafness, autosomal dominant 48 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> 607841 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> DFNA48 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> 607841 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/650?start=-3&limit=10&highlight=650"> 12q21.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617663"> Deafness, autosomal dominant 73 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617663"> 617663 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603317"> PTPRQ </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603317"> 603317 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/666?start=-3&limit=10&highlight=666"> 12q21.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616697"> Deafness, autosomal dominant 69, unilateral or asymmetric </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616697"> 616697 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/184745"> KITLG </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/184745"> 184745 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/719?start=-3&limit=10&highlight=719"> 12q23.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605583"> Deafness, autosomal dominant 25 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605583"> 605583 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607557"> SLC17A8 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607557"> 607557 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/906?start=-3&limit=10&highlight=906"> 12q24.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614152"> Deafness, autosomal dominant 64 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614152"> 614152 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605219"> DIABLO </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605219"> 605219 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/964?start=-3&limit=10&highlight=964"> 12q24.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608224"> Deafness, autosomal dominant 41 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608224"> 608224 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600844"> P2RX2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600844"> 600844 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/13/15?start=-3&limit=10&highlight=15"> 13q12.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601544"> Deafness, autosomal dominant 3A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601544"> 601544 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/121011"> GJB2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/121011"> 121011 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/13/16?start=-3&limit=10&highlight=16"> 13q12.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612643"> Deafness, autosomal dominant 3B </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612643"> 612643 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604418"> GJB6 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604418"> 604418 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/13/319?start=-3&limit=10&highlight=319"> 13q34 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619810"> Deafness, autosomal dominant 84 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619810"> 619810 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605868"> ATP11A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605868"> 605868 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/6?start=-3&limit=10&highlight=6"> 14q11.2-q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> Deafness, autosomal dominant 53 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> 609965 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> DFNA53 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> 609965 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/149?start=-3&limit=10&highlight=149"> 14q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601369"> Deafness, autosomal dominant 9 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601369"> 601369 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603196"> COCH </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603196"> 603196 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/287?start=-3&limit=10&highlight=287"> 14q23.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605192"> Deafness, autosomal dominant 23 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605192"> 605192 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601205"> SIX1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601205"> 601205 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/214?start=-3&limit=10&highlight=214"> 15q21.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617605"> ?Deafness, autosomal dominant 71 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617605"> 617605 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612186"> DMXL2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612186"> 612186 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/419?start=-3&limit=10&highlight=419"> 15q25-q26 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> Deafness, autosomal dominant 30 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> 606451 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> DFNA30 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> 606451 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/458?start=-3&limit=10&highlight=458"> 15q25.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616707"> ?Deafness, autosomal dominant 68 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616707"> 616707 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604799"> HOMER2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604799"> 604799 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/108?start=-3&limit=10&highlight=108"> 16p13.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616044"> Deafness, autosomal dominant 65 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616044"> 616044 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613577"> TBC1D24 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613577"> 613577 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/222?start=-3&limit=10&highlight=222"> 16p13.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618915"> ?Deafness, autosomal dominant 77 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618915"> 618915 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/158343"> ABCC1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/158343"> 158343 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/259?start=-3&limit=10&highlight=259"> 16p12.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616357"> Deafness, autosomal dominant 40 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616357"> 616357 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/123740"> CRYM </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/123740"> 123740 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/1031?start=-3&limit=10&highlight=1031"> 17q25.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604717"> Deafness, autosomal dominant 20/26 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604717"> 604717 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/102560"> ACTG1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/102560"> 102560 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/18/14?start=-3&limit=10&highlight=14"> 18p11.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620280"> ?Deafness, autosomal dominant 86 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620280"> 620280 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606930"> THOC1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606930"> 606930 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/18/80?start=-3&limit=10&highlight=80"> 18q11.1-q11.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619274"> Deafness, autosomal dominant 80 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619274"> 619274 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617782"> GREB1L </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617782"> 617782 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/19/797?start=-3&limit=10&highlight=797"> 19q13.31-q13.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614614"> Deafness, autosomal dominant 4B </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614614"> 614614 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614591"> CEACAM16 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614591"> 614591 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/19/977?start=-3&limit=10&highlight=977"> 19q13.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600652"> Deafness, autosomal dominant 4A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600652"> 600652 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608568"> MYH14 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608568"> 608568 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/20/445?start=-3&limit=10&highlight=445"> 20q13.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616340"> Deafness, autosomal dominant 67 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616340"> 616340 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606731"> OSBPL2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606731"> 606731 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/22/222?start=-3&limit=10&highlight=222"> 22q12.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603622"> Deafness, autosomal dominant 17 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603622"> 603622 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/160775"> MYH9 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/160775"> 160775 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
Not Mapped
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> Deafness, autosomal dominant 33 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> 614211 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> DFNA33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> 614211 </a>
</span>
</td>
</tr>
</tbody>
</table>
</div>
<div class="text-right small">
<a href="#mimPhenotypicSeriesFold_1" data-toggle="collapse">▲ Close</a>
</div>
</div>
</div>
<div id="mimLinksFold_1" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding ">
<caption>
Links
</caption>
<tbody>
<tr>
<td>
<dl>
<dt>Testing</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=612643[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=12046&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Clinical Resources</dt>
<dd><a href="https://clinicaltrials.gov/search?cond=(DEAFNESS, AUTOSOMAL DOMINANT) OR (GJB6)" class="mim-tip-hint" title="Clinical Trials" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Clinical Trials', 'domain': 'clinicaltrials.gov'})">Clinical Trials</a></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=12046&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/books/NBK1434/" class="mim-tip-hint" title="Expert-authored, peer-reviewed descriptions of inherited disorders including the uses of genetic testing in diagnosis, management, and genetic counseling." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Gene Reviews', 'domain': 'ncbi.nlm.nih.gov'})">Gene Reviews</a></dd>
<dd><a href="https://www.diseaseinfosearch.org/x/8145" class="mim-tip-hint" title="Network of disease-specific advocacy organizations, universities, private companies, government agencies, and public policy organizations." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Genetic Alliance', 'domain': 'diseaseinfosearch.org'})">Genetic Alliance</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=612643[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=90635" class="mim-tip-hint" title="European reference portal for information on rare diseases and orphan drugs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">OrphaNet</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Animal Models</dt>
<dd><a href="https://www.alliancegenome.org/disease/DOID:0110565" class="mim-tip-hint" title="Search Across Species; explore model organism and human comparative genomics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Alliance Genome', 'domain': 'alliancegenome.org'})">Alliance Genome</a></dd>
<dd><a href="http://www.informatics.jax.org/disease/612643" class="mim-tip-hint" title="Phenotypes, alleles, and disease models from Mouse Genome Informatics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MGI Mouse Phenotype', 'domain': 'informatics.jax.org'})">MGI Mouse Phenotype</a></dd>
</dl>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimLinksFold_1" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimDisorderCodesFold_1" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding">
<caption>
ICD+
</caption>
<tbody>
<tr>
<td>
<dl>
<dd>ORPHA: 90635</dd>
<dd>DO: 0110565</dd>
</dl>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimDisorderCodesFold_1" data-toggle="collapse">▲ Close</a>
</div>
</div>
</div>
</div>
<div class="row">
<p />
</div>
<div class="row">
<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
2:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<a href="/entry/601544?search=121011%20601544%20604418%20612643&highlight=121011%2C601544%2C604418%2C612643">
<span class="mim-tip-hint" title="Phenotype description, molecular basis known">
<span class="text-danger"><strong>#</strong></span>
601544.
</span>
DEAFNESS, AUTOSOMAL DOMINANT 3A; DFNA3A
</a>
</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">
<a href="/geneMap/13/15?start=-3&limit=10&highlight=15">
13q12.11</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">601544</span></span>
<br />
<a href="#mimPhenotypeMapFold_2" id="mimPhenotypeMapToggle_2" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'GeneMap'})"><span class="small"><span id="mimPhenotypeMapToggleTriangle_2" class="mimPingletonToggleTriangle" style="color: DarkOrchid">►</span> Phenotype-Gene Relationships</span></a>
<a href="#mimPhenotypicSeriesFold_2" id="mimPhenotypicSeriesToggle_2" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'PhenotypicSeries'})"><span class="small"><span id="mimPhenotypicSeriesToggleTriangle_2" class="mimSingletonToggleTriangle" style="color: #47B7D9">►</span> Phenotypic Series</span></a>
<a href="#mimDisorderCodesFold_2" id="mimDisorderCodesToggle_2" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'ICD+'})"><span class="small"><span id="mimDisorderCodesToggleTriangle_2" class="mimSingletonToggleTriangle" style="color: DarkRed">►</span> ICD+</span></a>
<a href="#mimLinksFold_2" id="mimLinksToggle_2" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'Links'})"><span class="small"><span id="mimLinksToggleTriangle_2" class="mimSingletonToggleTriangle" style="color: #337CB5">►</span> Links</span></a>
<div id="mimPhenotypeMapFold_2" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-bordered table-condensed small mim-table-padding">
<caption>
Phenotype-Gene Relationships
</caption>
<thead>
<tr>
<th>
Location
</th>
<th>
Phenotype
</th>
<th>
Phenotype <br /> MIM number
</th>
<th>
Inheritance
</th>
<th>
Phenotype <br /> mapping key
</th>
<th>
Gene/Locus
</th>
<th>
Gene/Locus <br /> MIM number
</th>
</tr>
</thead>
<tbody>
<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">
Deafness, autosomal dominant 3A
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601544"> 601544 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
GJB2
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/121011"> 121011 </a>
</span>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimPhenotypeMapFold_2" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimPhenotypicSeriesFold_2" class="well well-sm collapse mimSingletonToggleFold">
<div class="small">
<div class="row">
<div class="col-lg-12 col-md-12 col-sm-12 col-xs-12">
<h5>
Deafness, autosomal dominant
- <a href="/phenotypicSeries/PS124900">PS124900</a>
- 75 Entries
</h5>
</div>
</div>
<div class="row" style="margin-left: 0.125em; margin-right: 0.125em;">
<table class="table table-bordered table-condensed table-hover mim-table-padding">
<thead>
<tr>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Location</strong>
</th>
<th class="col-lg-5 col-md-5 col-sm-5 col-xs-6 text-nowrap">
<strong>Phenotype</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Inheritance</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Phenotype<br />mapping key</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Phenotype<br />MIM number</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Gene/Locus</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Gene/Locus<br />MIM number</strong>
</th>
</tr>
</thead>
<tbody>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/253?start=-3&limit=10&highlight=253"> 1p36.12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620227"> Deafness, autosomal dominant 85 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620227"> 620227 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617445"> USP48 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617445"> 617445 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/423?start=-3&limit=10&highlight=423"> 1p34.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612644"> Deafness, autosomal dominant 2B, with or without peripheral neuropathy </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612644"> 612644 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603324"> GJB3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603324"> 603324 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/456?start=-3&limit=10&highlight=456"> 1p34.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620283"> ?Deafness, autosomal dominant 88 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620283"> 620283 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611123"> EPHA10 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611123"> 611123 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/495?start=-3&limit=10&highlight=495"> 1p34.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600101"> Deafness, autosomal dominant 2A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600101"> 600101 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603537"> KCNQ4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603537"> 603537 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/847?start=-3&limit=10&highlight=847"> 1p21.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618533"> Deafness, autosomal dominant 37 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618533"> 618533 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120280"> COL11A1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120280"> 120280 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/997?start=-3&limit=10&highlight=997"> 1q21-q23 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> Deafness, autosomal dominant 49 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> 608372 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> DFNA49 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608372"> 608372 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1096?start=-3&limit=10&highlight=1096"> 1q21.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620281"> Deafness, autosomal dominant 87 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620281"> 620281 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602758"> PI4KB </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602758"> 602758 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1373?start=-3&limit=10&highlight=1373"> 1q23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601412"> Deafness, autosomal dominant 7 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601412"> 601412 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600298"> LMX1A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600298"> 600298 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1862?start=-3&limit=10&highlight=1862"> 1q44 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617772"> Deafness, autosomal dominant 34, with or without inflammation </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617772"> 617772 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606416"> NLRP3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606416"> 606416 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/205?start=-3&limit=10&highlight=205"> 2p21-p12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> Deafness, autosomal dominant 58 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="4 - A contiguous gene duplication or deletion syndrome in which multiple genes are involved"> 4 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> 615654 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> DFNA58 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615654"> 615654 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/396?start=-3&limit=10&highlight=396"> 2p12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> Deafness, autosomal dominant 43 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> 608394 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> DFNA43 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608394"> 608394 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/421?start=-3&limit=10&highlight=421"> 2p11.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619500"> ?Deafness, autosomal dominant 81 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619500"> 619500 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615427"> ELMOD3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615427"> 615427 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/675?start=-3&limit=10&highlight=675"> 2q23-q24.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> Deafness, autosomal dominant 16 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> 603964 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> DFNA16 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603964"> 603964 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/58?start=-3&limit=10&highlight=58"> 3p25.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619804"> Deafness, autosomal dominant 82 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619804"> 619804 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/108733"> ATP2B2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/108733"> 108733 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/643?start=-3&limit=10&highlight=643"> 3q21.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616968"> ?Deafness, autosomal dominant 70 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616968"> 616968 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/116945"> MCM2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/116945"> 116945 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/665?start=-3&limit=10&highlight=665"> 3q22 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> Deafness, autosomal dominant 18 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> 606012 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> DFNA18 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606012"> 606012 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/745?start=-3&limit=10&highlight=745"> 3q23 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618787"> Deafness, autosomal dominant 76 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618787"> 618787 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602734"> PLS1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602734"> 602734 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/966?start=-3&limit=10&highlight=966"> 3q28 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607453"> ?Deafness, autosomal dominant 44 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607453"> 607453 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611051"> CCDC50 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611051"> 611051 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/69?start=-3&limit=10&highlight=69"> 4p16.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600965"> Deafness, autosomal dominant 6/14/38 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600965"> 600965 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606201"> WFS1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606201"> 606201 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/243?start=-3&limit=10&highlight=243"> 4q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612431"> Deafness, autosomal dominant 27 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612431"> 612431 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600571"> REST </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600571"> 600571 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/365?start=-3&limit=10&highlight=365"> 4q21.22 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619086"> ?Deafness, autosomal dominant 79 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619086"> 619086 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608370"> SCD5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608370"> 608370 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/415?start=-3&limit=10&highlight=415"> 4q22.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620284"> ?Deafness, autosomal dominant 89 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620284"> 620284 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601461"> ATOH1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601461"> 601461 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/696?start=-3&limit=10&highlight=696"> 4q35-qter </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> Deafness, autosomal dominant 24 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> 606282 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> DFNA24 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606282"> 606282 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/239?start=-3&limit=10&highlight=239"> 5q13.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619808"> ?Deafness, autosomal dominant 83 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619808"> 619808 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/157129"> MAP1B </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/157129"> 157129 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/412?start=-3&limit=10&highlight=412"> 5q23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619081"> Deafness, autosomal dominant 78 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619081"> 619081 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600840"> SLC12A2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600840"> 600840 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/424?start=-3&limit=10&highlight=424"> 5q31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> Deafness, autosomal dominant 54 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> 615649 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> DFNA54 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615649"> 615649 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/605?start=-3&limit=10&highlight=605"> 5q31.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/124900"> Deafness, autosomal dominant 1, with or without thrombocytopenia </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/124900"> 124900 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602121"> DIAPH1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602121"> 602121 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/630?start=-3&limit=10&highlight=630"> 5q32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602459"> Deafness, autosomal dominant 15/52 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602459"> 602459 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602460"> POU4F3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602460"> 602460 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/119?start=-3&limit=10&highlight=119"> 6p22.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607017"> Deafness, autosomal dominant 21 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607017"> 607017 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611410"> RIPOR2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611410"> 611410 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/245?start=-3&limit=10&highlight=245"> 6p21.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> Deafness, autosomal dominant 31 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> 608645 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> DFNA31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608645"> 608645 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/340?start=-3&limit=10&highlight=340"> 6p21.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617606"> ?Deafness, autosomal dominant 72 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617606"> 617606 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606107"> SLC44A4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606107"> 606107 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/383?start=-3&limit=10&highlight=383"> 6p21.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601868"> Deafness, autosomal dominant 13 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601868"> 601868 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120290"> COL11A2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120290"> 120290 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/658?start=-3&limit=10&highlight=658"> 6q14.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> Deafness, autosomal dominant 22 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> 606346 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> MYO6 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> 600970 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/658?start=-3&limit=10&highlight=658"> 6q14.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606346"> 606346 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> MYO6 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600970"> 600970 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/764?start=-3&limit=10&highlight=764"> 6q21 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616969"> ?Deafness, autosomal dominant 66 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616969"> 616969 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603356"> CD164 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603356"> 603356 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/874?start=-3&limit=10&highlight=874"> 6q23.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601316"> Deafness, autosomal dominant 10 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601316"> 601316 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603550"> EYA4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603550"> 603550 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/120?start=-3&limit=10&highlight=120"> 7p15.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600994"> Deafness, autosomal dominant 5 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600994"> 600994 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608798"> GSDME </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608798"> 608798 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/172?start=-3&limit=10&highlight=172"> 7p14.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618140"> ?Deafness, autosomal dominant 74 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618140"> 618140 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602987"> PDE1C </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602987"> 602987 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/457?start=-3&limit=10&highlight=457"> 7q22.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618778"> ?Deafness, autosomal dominant 75 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618778"> 618778 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603015"> TRRAP </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603015"> 603015 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/7/671?start=-3&limit=10&highlight=671"> 7q32.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613074"> Deafness, autosomal dominant 50 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613074"> 613074 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611606"> MIR96 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611606"> 611606 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/8/450?start=-3&limit=10&highlight=450"> 8q22.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608641"> Deafness, autosomal dominant 28 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608641"> 608641 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608576"> GRHL2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608576"> 608576 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/52?start=-3&limit=10&highlight=52"> 9p22-p21 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> Deafness, autosomal dominant 47 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> 608652 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> DFNA47 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608652"> 608652 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/216?start=-3&limit=10&highlight=216"> 9q21.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> Deafness, autosomal dominant 51 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="4 - A contiguous gene duplication or deletion syndrome in which multiple genes are involved"> 4 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> 613558 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> DFNA51 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613558"> 613558 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/243?start=-3&limit=10&highlight=243"> 9q21.13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606705"> Deafness, autosomal dominant 36 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606705"> 606705 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606706"> TMC1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606706"> 606706 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/448?start=-3&limit=10&highlight=448"> 9q33.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615629"> Deafness, autosomal dominant 56 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615629"> 615629 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/187380"> TNC </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/187380"> 187380 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/10/112?start=-3&limit=10&highlight=112"> 10p12.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620722"> Deafness, autosomal dominant 90 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620722"> 620722 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606808"> MYO3A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606808"> 606808 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/250?start=-3&limit=10&highlight=250"> 11p14.2-q12.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> Deafness, autosomal dominant 59 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> 612642 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> DFNA59 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612642"> 612642 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/775?start=-3&limit=10&highlight=775"> 11q13.5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601317"> Deafness, autosomal dominant 11 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601317"> 601317 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/276903"> MYO7A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/276903"> 276903 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/1026?start=-3&limit=10&highlight=1026"> 11q23.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601543"> Deafness, autosomal dominant 8/12 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601543"> 601543 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602574"> TECTA </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602574"> 602574 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/309?start=-3&limit=10&highlight=309"> 12q13-q14 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> Deafness, autosomal dominant 48 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> 607841 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> DFNA48 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607841"> 607841 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/650?start=-3&limit=10&highlight=650"> 12q21.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617663"> Deafness, autosomal dominant 73 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617663"> 617663 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603317"> PTPRQ </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603317"> 603317 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/666?start=-3&limit=10&highlight=666"> 12q21.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616697"> Deafness, autosomal dominant 69, unilateral or asymmetric </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616697"> 616697 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/184745"> KITLG </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/184745"> 184745 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/719?start=-3&limit=10&highlight=719"> 12q23.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605583"> Deafness, autosomal dominant 25 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605583"> 605583 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607557"> SLC17A8 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607557"> 607557 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/906?start=-3&limit=10&highlight=906"> 12q24.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614152"> Deafness, autosomal dominant 64 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614152"> 614152 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605219"> DIABLO </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605219"> 605219 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/964?start=-3&limit=10&highlight=964"> 12q24.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608224"> Deafness, autosomal dominant 41 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608224"> 608224 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600844"> P2RX2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600844"> 600844 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/13/15?start=-3&limit=10&highlight=15"> 13q12.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601544"> Deafness, autosomal dominant 3A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601544"> 601544 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/121011"> GJB2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/121011"> 121011 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/13/16?start=-3&limit=10&highlight=16"> 13q12.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612643"> Deafness, autosomal dominant 3B </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612643"> 612643 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604418"> GJB6 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604418"> 604418 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/13/319?start=-3&limit=10&highlight=319"> 13q34 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619810"> Deafness, autosomal dominant 84 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619810"> 619810 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605868"> ATP11A </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605868"> 605868 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/6?start=-3&limit=10&highlight=6"> 14q11.2-q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> Deafness, autosomal dominant 53 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> 609965 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> DFNA53 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609965"> 609965 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/149?start=-3&limit=10&highlight=149"> 14q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601369"> Deafness, autosomal dominant 9 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601369"> 601369 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603196"> COCH </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603196"> 603196 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/287?start=-3&limit=10&highlight=287"> 14q23.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605192"> Deafness, autosomal dominant 23 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605192"> 605192 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601205"> SIX1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601205"> 601205 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/214?start=-3&limit=10&highlight=214"> 15q21.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617605"> ?Deafness, autosomal dominant 71 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617605"> 617605 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612186"> DMXL2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612186"> 612186 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/419?start=-3&limit=10&highlight=419"> 15q25-q26 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> Deafness, autosomal dominant 30 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> 606451 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> DFNA30 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606451"> 606451 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/458?start=-3&limit=10&highlight=458"> 15q25.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616707"> ?Deafness, autosomal dominant 68 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616707"> 616707 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604799"> HOMER2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604799"> 604799 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/108?start=-3&limit=10&highlight=108"> 16p13.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616044"> Deafness, autosomal dominant 65 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616044"> 616044 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613577"> TBC1D24 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613577"> 613577 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/222?start=-3&limit=10&highlight=222"> 16p13.11 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618915"> ?Deafness, autosomal dominant 77 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/618915"> 618915 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/158343"> ABCC1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/158343"> 158343 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/259?start=-3&limit=10&highlight=259"> 16p12.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616357"> Deafness, autosomal dominant 40 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616357"> 616357 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/123740"> CRYM </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/123740"> 123740 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/1031?start=-3&limit=10&highlight=1031"> 17q25.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604717"> Deafness, autosomal dominant 20/26 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604717"> 604717 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/102560"> ACTG1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/102560"> 102560 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/18/14?start=-3&limit=10&highlight=14"> 18p11.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620280"> ?Deafness, autosomal dominant 86 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620280"> 620280 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606930"> THOC1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606930"> 606930 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/18/80?start=-3&limit=10&highlight=80"> 18q11.1-q11.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619274"> Deafness, autosomal dominant 80 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/619274"> 619274 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617782"> GREB1L </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/617782"> 617782 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/19/797?start=-3&limit=10&highlight=797"> 19q13.31-q13.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614614"> Deafness, autosomal dominant 4B </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614614"> 614614 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614591"> CEACAM16 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614591"> 614591 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/19/977?start=-3&limit=10&highlight=977"> 19q13.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600652"> Deafness, autosomal dominant 4A </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600652"> 600652 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608568"> MYH14 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608568"> 608568 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/20/445?start=-3&limit=10&highlight=445"> 20q13.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616340"> Deafness, autosomal dominant 67 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/616340"> 616340 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606731"> OSBPL2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606731"> 606731 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/22/222?start=-3&limit=10&highlight=222"> 22q12.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603622"> Deafness, autosomal dominant 17 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603622"> 603622 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/160775"> MYH9 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/160775"> 160775 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
Not Mapped
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> Deafness, autosomal dominant 33 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> 614211 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> DFNA33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614211"> 614211 </a>
</span>
</td>
</tr>
</tbody>
</table>
</div>
<div class="text-right small">
<a href="#mimPhenotypicSeriesFold_2" data-toggle="collapse">▲ Close</a>
</div>
</div>
</div>
<div id="mimLinksFold_2" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding ">
<caption>
Links
</caption>
<tbody>
<tr>
<td>
<dl>
<dt>Testing</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=601544[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=12046&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Clinical Resources</dt>
<dd><a href="https://clinicaltrials.gov/search?cond=(DEAFNESS, AUTOSOMAL DOMINANT) OR (GJB2)" class="mim-tip-hint" title="Clinical Trials" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Clinical Trials', 'domain': 'clinicaltrials.gov'})">Clinical Trials</a></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=12046&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/books/NBK1434/" class="mim-tip-hint" title="Expert-authored, peer-reviewed descriptions of inherited disorders including the uses of genetic testing in diagnosis, management, and genetic counseling." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Gene Reviews', 'domain': 'ncbi.nlm.nih.gov'})">Gene Reviews</a></dd>
<dd><a href="https://www.diseaseinfosearch.org/x/8144" class="mim-tip-hint" title="Network of disease-specific advocacy organizations, universities, private companies, government agencies, and public policy organizations." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Genetic Alliance', 'domain': 'diseaseinfosearch.org'})">Genetic Alliance</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=601544[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=90635" class="mim-tip-hint" title="European reference portal for information on rare diseases and orphan drugs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">OrphaNet</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Animal Models</dt>
<dd><a href="https://www.alliancegenome.org/disease/DOID:0110564" class="mim-tip-hint" title="Search Across Species; explore model organism and human comparative genomics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Alliance Genome', 'domain': 'alliancegenome.org'})">Alliance Genome</a></dd>
<dd><a href="http://www.informatics.jax.org/disease/601544" class="mim-tip-hint" title="Phenotypes, alleles, and disease models from Mouse Genome Informatics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MGI Mouse Phenotype', 'domain': 'informatics.jax.org'})">MGI Mouse Phenotype</a></dd>
</dl>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimLinksFold_2" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimDisorderCodesFold_2" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding">
<caption>
ICD+
</caption>
<tbody>
<tr>
<td>
<dl>
<dd>ORPHA: 90635</dd>
<dd>DO: 0110564</dd>
</dl>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimDisorderCodesFold_2" data-toggle="collapse">▲ Close</a>
</div>
</div>
</div>
</div>
<div class="row">
<p />
</div>
<div class="row">
<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
3:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<a href="/entry/121011?search=121011%20601544%20604418%20612643&highlight=121011%2C601544%2C604418%2C612643">
<span class="mim-tip-hint" title="Gene description">
<span class="text-danger"><strong>*</strong></span>
121011.
</span>
GAP JUNCTION PROTEIN, BETA-2; GJB2
</a>
</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">
<a href="/geneMap/13/15?start=-3&limit=10&highlight=15">
13q12.11</a></span>,
Genomic coordinates <span class="small">(GRCh38)</span>: <span class="mim-font"><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&position=chr13:20187470-20192938&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'})">13:20,187,470-20,192,938</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">121011</span></span>
<br />
<a href="#mimGeneMapFold_3" id="mimGeneMapToggle_3" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'GeneMap'})"><span class="small"><span id="mimGeneMapToggleTriangle_3" class="mimSingletonToggleTriangle" style="color: DarkOrchid">►</span> Gene-Phenotype Relationships</span></a>
<a href="#mimDisorderCodesFold_3" id="mimDisorderCodesToggle_3" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'ICD+'})"><span class="small"><span id="mimDisorderCodesToggleTriangle_3" class="mimSingletonToggleTriangle" style="color: DarkRed">►</span> ICD+</span></a>
<a href="#mimLinksFold_3" id="mimLinksToggle_3" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'Links'})"><span class="small"><span id="mimLinksToggleTriangle_3" class="mimSingletonToggleTriangle" style="color: #337CB5">►</span> Links</span></a>
<div id="mimGeneMapFold_3" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-bordered table-condensed small mim-table-padding">
<caption>
Gene-Phenotype Relationships
</caption>
<thead>
<tr>
<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="7">
<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">
Bart-Pumphrey syndrome
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/149200"> 149200 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
Deafness, autosomal dominant 3A
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601544"> 601544 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
Deafness, autosomal recessive 1A
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/220290"> 220290 </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>
</tr>
<tr>
<td>
<span class="mim-font">
Hystrix-like ichthyosis with deafness
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602540"> 602540 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
Keratitis-ichthyosis-deafness syndrome
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/148210"> 148210 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
Keratoderma, palmoplantar, with deafness
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/148350"> 148350 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
Vohwinkel syndrome
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/124500"> 124500 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimGeneMapFold_3" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimLinksFold_3" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding ">
<caption>
Links
</caption>
<tbody>
<tr>
<td>
<dl>
<dt>Testing</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=121011[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Genome</dt>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Location/View?db=core;g=ENSG00000165474;t=ENST00000382848" class="mim-tip-hint" title="Genome databases for vertebrates and other eukaryotic species." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Ensembl', 'domain': 'ensembl.org'})">Ensembl</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/genome/gdv/browser/gene/?id=2706" class="mim-tip-hint" title="Detailed views of the complete genomes of selected organisms from vertebrates to protozoa." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Genome Viewer', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Genome Viewer</a></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&hgFind=omimGeneAcc&position=121011" 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'})">UCSC Genome Browser</a></dd>
</dl>
</td>
<td>
<dl>
<dt>DNA</dt>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Transcript/Sequence_cDNA?db=core;g=ENSG00000165474;t=ENST00000382848" class="mim-tip-hint" title="Transcript-based views for coding and noncoding DNA." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Ensembl', 'domain': 'ensembl.org'})">Ensembl (MANE Select)</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_004004,XM_011535049" class="mim-tip-hint" title="A collection of genome, gene, and transcript sequence data from several sources, including GenBank, RefSeq." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI RefSeq', 'domain': 'ncbi.nlm.nih'})">NCBI RefSeq</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_004004" class="mim-tip-hint" title="A collection of genome, gene, and transcript sequence data from several sources, including GenBank, RefSeq." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI RefSeq (MANE)', 'domain': 'ncbi.nlm.nih'})">NCBI RefSeq (MANE Select)</a></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&hgFind=omimGeneAcc&position=121011" 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'})">UCSC Genome Browser</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Protein</dt>
<dd><a href="https://hprd.org/summary?hprd_id=00413&isoform_id=00413_1&isoform_name=Isoform_1" class="mim-tip-hint" title="The Human Protein Reference Database; manually extracted and visually depicted information on human proteins." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'HPRD', 'domain': 'hprd.org'})">HPRD</a></dd>
<dd><a href="https://www.proteinatlas.org/search/GJB2" class="mim-tip-hint" title="The Human Protein Atlas contains information for a large majority of all human protein-coding genes regarding the expression and localization of the corresponding proteins based on both RNA and protein data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'HumanProteinAtlas', 'domain': 'proteinatlas.org'})">Human Protein Atlas</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/protein/4262722,4481753,9652207,16877592,19401867,30582303,30720310,33391197,37620517,37620519,37620521,37620523,37620525,37620527,37620529,37620531,37620533,42558283,47938211,62999482,62999486,77416855,116294889,119628657,119628658,189069329,381414125,381414127,532642932,532642934,559148900,588269636,767977602,1377672464,1561851419,1562483768,1562483770,1562483772,1562483774,1562483776,1562483778,1562483780,1562483782,1562483784,1562483786,1562483788,1562483790,1562483792,1562483794,1562483796,1562483798,1562483800,1562483802,1562483804,1562483806,1562483808,1562483810,1562483812,1562483814,1562483816,1562483818,1562483820,1562483822,1562483824,1562483826,1562483828,1562483830,1562483832,1562483834,1562483836,1562483838,1562483840,1562483842,1562483844,1562483846,1562483848,1562483850,1562483852,1562483854,1562483856,1562483858,1562483860,1562483862,1562483864,1562483866,1562483868,1562483870,1562483872,1562483874,1562483876,1562483878,1562483880,1562483882,1569137587,1569137589,2030916096,2327866302,2462536941" class="mim-tip-hint" title="NCBI protein data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Protein', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Protein</a></dd>
<dd><a href="https://www.uniprot.org/uniprotkb/P29033" class="mim-tip-hint" title="Comprehensive protein sequence and functional information, including supporting data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'UniProt', 'domain': 'uniprot.org'})">UniProt</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Gene Info</dt>
<dd><a href="http://biogps.org/#goto=genereport&id=2706" 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></dd>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Gene/Summary?db=core;g=ENSG00000165474;t=ENST00000382848" class="mim-tip-hint" title="Orthologs, paralogs, regulatory regions, and splice variants." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Ensembl', 'domain': 'ensembl.org'})">Ensembl</a></dd>
<dd><a href="https://www.genecards.org/cgi-bin/carddisp.pl?gene=GJB2" class="mim-tip-hint" title="The Human Genome Compendium; web-based cards integrating automatically mined information on human genes." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GeneCards', 'domain': 'genecards.org'})">GeneCards</a></dd>
<dd><a href="http://amigo.geneontology.org/amigo/search/annotation?q=GJB2" class="mim-tip-hint" title="Terms, defined using controlled vocabulary, representing gene product properties (biologic process, cellular component, molecular function) across species." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GeneOntology', 'domain': 'amigo.geneontology.org'})">Gene Ontology</a></dd>
<dd><a href="https://www.genome.jp/dbget-bin/www_bget?hsa+2706" 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></dd>
<dd><a href="http://v1.marrvel.org/search/gene/GJB2" class="mim-tip-hint" title="Model organism Aggregated Resources for Rare Variant ExpLoration." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MARRVEL', 'domain': 'marrvel.org'})">MARRVEL</a></dd>
<dd><a href="https://monarchinitiative.org/NCBIGene:2706" class="mim-tip-hint" title="Monarch Initiative." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Monarch', 'domain': 'monarchinitiative.org'})">Monarch</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gene/2706" 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></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgGene?db=hg38&hgg_chrom=chr13&hgg_gene=ENST00000382848.5&hgg_start=20187470&hgg_end=20192938&hgg_type=knownGene" class="mim-tip-hint" title="UCSC Genome Bioinformatics; gene-specific structure and function information with links to other databases." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'UCSC', 'domain': 'genome.ucsc.edu'})">UCSC</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Clinical Resources</dt>
<dd><a href="https://search.clinicalgenome.org/kb/gene-dosage/HGNC:4284" class="mim-tip-hint" title="A ClinGen curated resource of genes and regions of the genome that are dosage sensitive and should be targeted on a cytogenomic array." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ClinGen Dosage', 'domain': 'dosage.clinicalgenome.org'})">ClinGen Dosage</a></dd>
<dd><a href="https://search.clinicalgenome.org/kb/genes/HGNC:4284" class="mim-tip-hint" title="A ClinGen curated resource of ratings for the strength of evidence supporting or refuting the clinical validity of the claim(s) that variation in a particular gene causes disease." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ClinGen Validity', 'domain': 'search.clinicalgenome.org'})">ClinGen Validity</a></dd>
<dd><a href="https://medlineplus.gov/genetics/gene/gjb2" class="mim-tip-hint" title="Consumer-friendly information about the effects of genetic variation on human health." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MedlinePlus Genetics', 'domain': 'medlineplus.gov'})">MedlinePlus Genetics</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=121011[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Variation</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/clinvar?term=121011[MIM]" class="mim-tip-hint" title="ClinVar aggregates information about sequence variation and its relationship to human health." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ClinVar', 'domain': 'ncbi.nlm.nih.gov'})">ClinVar</a></dd>
<dd><a href="https://www.deciphergenomics.org/gene/GJB2/overview/clinical-info" class="mim-tip-hint" title="DECIPHER" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'DECIPHER', 'domain': 'DECIPHER'})">DECIPHER</a></dd>
<dd><a href="https://gnomad.broadinstitute.org/gene/ENSG00000165474" class="mim-tip-hint" title="The Genome Aggregation Database (gnomAD), Broad Institute." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'gnomAD', 'domain': 'gnomad.broadinstitute.org'})">gnomAD</a></dd>
<dd><a href="https://www.ebi.ac.uk/gwas/search?query=GJB2" class="mim-tip-hint" title="GWAS Catalog; NHGRI-EBI Catalog of published genome-wide association studies." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GWAS Catalog', 'domain': 'gwascatalog.org'})">GWAS Catalog </a></dd>
<dd><a href="https://www.gwascentral.org/search?q=GJB2" class="mim-tip-hint" title="GWAS Central; summary level genotype-to-phenotype information from genetic association studies." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GWAS Central', 'domain': 'gwascentral.org'})">GWAS Central </a></dd>
<dd><a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=GJB2" class="mim-tip-hint" title="Human Gene Mutation Database; published mutations causing or associated with human inherited disease; disease-associated/functional polymorphisms." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'HGMD', 'domain': 'hgmd.cf.ac.uk'})">HGMD</a></dd>
<dd>Locus Specific DBs</dd>
<dd style="margin-left: 0.5em;"><a href="http://davinci.crg.es/deafness/" title="The Connexin-deafness homepage" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">The Connexin-deafness home…</a></dd><dd style="margin-left: 0.5em;"><a href="http://webh01.ua.ac.be/hhh/" title="Hereditary Hearing Loss Homepage" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">Hereditary Hearing Loss Ho…</a></dd><dd style="margin-left: 0.5em;"><a href="http://www.umd.be/DFNB1-GJB2/" title="The UMD DFNB1-GJB2 mutations database" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">The UMD DFNB1-GJB2 mutatio…</a></dd><dd style="margin-left: 0.5em;"><a href="https://research.cchmc.org/LOVD2/home.php?select_db=GJB2" title="CCHMC - Human Genetics Mutation Database" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">CCHMC - Human Genetics Mut…</a></dd>
<dd><a href="https://evs.gs.washington.edu/EVS/PopStatsServlet?searchBy=Gene+Hugo&target=GJB2&upstreamSize=0&downstreamSize=0&x=0&y=0" class="mim-tip-hint" title="National Heart, Lung, and Blood Institute Exome Variant Server." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NHLBI EVS', 'domain': 'evs.gs.washington.edu'})">NHLBI EVS</a></dd>
<dd><a href="https://www.pharmgkb.org/gene/PA28695" class="mim-tip-hint" title="Pharmacogenomics Knowledge Base; curated and annotated information regarding the effects of human genetic variations on drug response." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PharmGKB', 'domain': 'pharmgkb.org'})">PharmGKB</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Animal Models</dt>
<dd><a href="https://www.alliancegenome.org/gene/HGNC:4284" class="mim-tip-hint" title="Search Across Species; explore model organism and human comparative genomics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Alliance Genome', 'domain': 'alliancegenome.org'})">Alliance Genome</a></dd>
<dd><a href="https://www.mousephenotype.org/data/genes/MGI:95720" class="mim-tip-hint" title="International Mouse Phenotyping Consortium." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'IMPC', 'domain': 'knockoutmouse.org'})">IMPC</a></dd>
<dd><a href="http://v1.marrvel.org/search/gene/GJB2#HomologGenesPanel" class="mim-tip-hint" title="Model organism Aggregated Resources for Rare Variant ExpLoration." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MARRVEL', 'domain': 'marrvel.org'})">MARRVEL</a></dd>
<dd><a href="http://www.informatics.jax.org/marker/MGI:95720" class="mim-tip-hint" title="Mouse Genome Informatics; international database resource for the laboratory mouse, including integrated genetic, genomic, and biological data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MGI Mouse Gene', 'domain': 'informatics.jax.org'})">MGI Mouse Gene</a></dd>
<dd><a href="https://www.mmrrc.org/catalog/StrainCatalogSearchForm.php?search_query=MGI:95720" class="mim-tip-hint" title="Mutant Mouse Resource & Research Centers." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MMRRC', 'domain': 'mmrrc.org'})">MMRRC</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gene/2706/ortholog/" class="mim-tip-hint" title="Orthologous genes at NCBI." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Orthologs', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Orthologs</a></dd>
<dd><a href="https://omia.org/OMIA002439/" class="mim-tip-hint" title="Online Mendelian Inheritance in Animals (OMIA) is a database of genes, inherited disorders and traits in 191 animal species (other than human and mouse.)" target="_blank">OMIA</a></dd>
<dd><a href="https://www.orthodb.org/?ncbi=2706" class="mim-tip-hint" title="Hierarchical catalogue of orthologs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrthoDB', 'domain': 'orthodb.org'})">OrthoDB</a></dd>
<dd><a href="https://zfin.org/ZDB-GENE-040406-1" class="mim-tip-hint" title="The Zebrafish Model Organism Database." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ZFin', 'domain': 'zfin.org'})">ZFin</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Cell Lines</dt>
<dd><a href="https://catalog.coriell.org/Search?q=OmimNum:121011" class="definition" title="Coriell Cell Repositories; cell cultures and DNA derived from cell cultures." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'CCR', 'domain': 'ccr.coriell.org'})">Coriell</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Cellular Pathways</dt>
<dd><a href="https://reactome.org/content/query?q=GJB2&species=Homo+sapiens&types=Reaction&types=Pathway&cluster=true" class="definition" title="Protein-specific information in the context of relevant cellular pathways." target="_blank" onclick="gtag('event', 'mim_outbound', {{'name': 'Reactome', 'domain': 'reactome.org'}})">Reactome</a></dd>
</dl>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimLinksFold_3" data-toggle="collapse">▲ Close</a>
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</div>
<div id="mimDisorderCodesFold_3" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding">
<caption>
ICD+
</caption>
<tbody>
<tr>
<td>
<dl>
<dd>SNOMEDCT: 1271009, 24559001, 2625009, 722203001</dd>
</dl>
</td>
</tr>
</tbody>
</table>
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<a href="#mimDisorderCodesFold_3" data-toggle="collapse">▲ Close</a>
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<div class="row">
<p />
</div>
<div class="row">
<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
4:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<a href="/entry/604418?search=121011%20601544%20604418%20612643&highlight=121011%2C601544%2C604418%2C612643">
<span class="mim-tip-hint" title="Gene description">
<span class="text-danger"><strong>*</strong></span>
604418.
</span>
GAP JUNCTION PROTEIN, BETA-6; GJB6
</a>
</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">
<a href="/geneMap/13/16?start=-3&limit=10&highlight=16">
13q12.11</a></span>,
Genomic coordinates <span class="small">(GRCh38)</span>: <span class="mim-font"><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&position=chr13:20221962-20232319&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'})">13:20,221,962-20,232,319</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">604418</span></span>
<br />
<a href="#mimGeneMapFold_4" id="mimGeneMapToggle_4" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'GeneMap'})"><span class="small"><span id="mimGeneMapToggleTriangle_4" class="mimSingletonToggleTriangle" style="color: DarkOrchid">►</span> Gene-Phenotype Relationships</span></a>
<a href="#mimDisorderCodesFold_4" id="mimDisorderCodesToggle_4" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'ICD+'})"><span class="small"><span id="mimDisorderCodesToggleTriangle_4" class="mimSingletonToggleTriangle" style="color: DarkRed">►</span> ICD+</span></a>
<a href="#mimLinksFold_4" id="mimLinksToggle_4" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'Links'})"><span class="small"><span id="mimLinksToggleTriangle_4" class="mimSingletonToggleTriangle" style="color: #337CB5">►</span> Links</span></a>
<div id="mimGeneMapFold_4" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-bordered table-condensed small mim-table-padding">
<caption>
Gene-Phenotype Relationships
</caption>
<thead>
<tr>
<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="4">
<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">
Deafness, autosomal dominant 3B
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612643"> 612643 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
Deafness, autosomal recessive 1B
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612645"> 612645 </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>
</tr>
<tr>
<td>
<span class="mim-font">
Deafness, digenic GJB2/GJB6
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/220290"> 220290 </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>
</tr>
<tr>
<td>
<span class="mim-font">
Ectodermal dysplasia 2, Clouston type
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/129500"> 129500 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimGeneMapFold_4" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimLinksFold_4" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding ">
<caption>
Links
</caption>
<tbody>
<tr>
<td>
<dl>
<dt>Testing</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=604418[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Genome</dt>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Location/View?db=core;g=ENSG00000121742;t=ENST00000647029" class="mim-tip-hint" title="Genome databases for vertebrates and other eukaryotic species." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Ensembl', 'domain': 'ensembl.org'})">Ensembl</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/genome/gdv/browser/gene/?id=10804" class="mim-tip-hint" title="Detailed views of the complete genomes of selected organisms from vertebrates to protozoa." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Genome Viewer', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Genome Viewer</a></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&hgFind=omimGeneAcc&position=604418" 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'})">UCSC Genome Browser</a></dd>
</dl>
</td>
<td>
<dl>
<dt>DNA</dt>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Transcript/Sequence_cDNA?db=core;g=ENSG00000121742;t=ENST00000647029" class="mim-tip-hint" title="Transcript-based views for coding and noncoding DNA." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Ensembl', 'domain': 'ensembl.org'})">Ensembl (MANE Select)</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_001110219,NM_001110220,NM_001110221,NM_001370090,NM_001370091,NM_001370092,NM_006783,XM_047430056,XM_047430057" class="mim-tip-hint" title="A collection of genome, gene, and transcript sequence data from several sources, including GenBank, RefSeq." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI RefSeq', 'domain': 'ncbi.nlm.nih'})">NCBI RefSeq</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_001110219" class="mim-tip-hint" title="A collection of genome, gene, and transcript sequence data from several sources, including GenBank, RefSeq." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI RefSeq (MANE)', 'domain': 'ncbi.nlm.nih'})">NCBI RefSeq (MANE Select)</a></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&hgFind=omimGeneAcc&position=604418" 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'})">UCSC Genome Browser</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Protein</dt>
<dd><a href="https://hprd.org/summary?hprd_id=05107&isoform_id=05107_1&isoform_name=Isoform_1" class="mim-tip-hint" title="The Human Protein Reference Database; manually extracted and visually depicted information on human proteins." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'HPRD', 'domain': 'hprd.org'})">HPRD</a></dd>
<dd><a href="https://www.proteinatlas.org/search/GJB6" class="mim-tip-hint" title="The Human Protein Atlas contains information for a large majority of all human protein-coding genes regarding the expression and localization of the corresponding proteins based on both RNA and protein data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'HumanProteinAtlas', 'domain': 'proteinatlas.org'})">Human Protein Atlas</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/protein/4127986,24660317,31580773,34978349,40254837,45503288,55925661,55925663,55925665,119628659,119628660,119628661,119628662,119628663,158260207,158966714,158966717,159032020,193786771,1625627209,1625627211,1625627213,2217293464,2217293466,2462536057,2462536059" class="mim-tip-hint" title="NCBI protein data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Protein', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Protein</a></dd>
<dd><a href="https://www.uniprot.org/uniprotkb/O95452" class="mim-tip-hint" title="Comprehensive protein sequence and functional information, including supporting data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'UniProt', 'domain': 'uniprot.org'})">UniProt</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Gene Info</dt>
<dd><a href="http://biogps.org/#goto=genereport&id=10804" 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></dd>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Gene/Summary?db=core;g=ENSG00000121742;t=ENST00000647029" class="mim-tip-hint" title="Orthologs, paralogs, regulatory regions, and splice variants." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Ensembl', 'domain': 'ensembl.org'})">Ensembl</a></dd>
<dd><a href="https://www.genecards.org/cgi-bin/carddisp.pl?gene=GJB6" class="mim-tip-hint" title="The Human Genome Compendium; web-based cards integrating automatically mined information on human genes." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GeneCards', 'domain': 'genecards.org'})">GeneCards</a></dd>
<dd><a href="http://amigo.geneontology.org/amigo/search/annotation?q=GJB6" class="mim-tip-hint" title="Terms, defined using controlled vocabulary, representing gene product properties (biologic process, cellular component, molecular function) across species." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GeneOntology', 'domain': 'amigo.geneontology.org'})">Gene Ontology</a></dd>
<dd><a href="https://www.genome.jp/dbget-bin/www_bget?hsa+10804" 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></dd>
<dd><a href="http://v1.marrvel.org/search/gene/GJB6" class="mim-tip-hint" title="Model organism Aggregated Resources for Rare Variant ExpLoration." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MARRVEL', 'domain': 'marrvel.org'})">MARRVEL</a></dd>
<dd><a href="https://monarchinitiative.org/NCBIGene:10804" class="mim-tip-hint" title="Monarch Initiative." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Monarch', 'domain': 'monarchinitiative.org'})">Monarch</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gene/10804" 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></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgGene?db=hg38&hgg_chrom=chr13&hgg_gene=ENST00000647029.1&hgg_start=20221962&hgg_end=20232319&hgg_type=knownGene" class="mim-tip-hint" title="UCSC Genome Bioinformatics; gene-specific structure and function information with links to other databases." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'UCSC', 'domain': 'genome.ucsc.edu'})">UCSC</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Clinical Resources</dt>
<dd><a href="https://search.clinicalgenome.org/kb/gene-dosage/HGNC:4288" class="mim-tip-hint" title="A ClinGen curated resource of genes and regions of the genome that are dosage sensitive and should be targeted on a cytogenomic array." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ClinGen Dosage', 'domain': 'dosage.clinicalgenome.org'})">ClinGen Dosage</a></dd>
<dd><a href="https://search.clinicalgenome.org/kb/genes/HGNC:4288" class="mim-tip-hint" title="A ClinGen curated resource of ratings for the strength of evidence supporting or refuting the clinical validity of the claim(s) that variation in a particular gene causes disease." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ClinGen Validity', 'domain': 'search.clinicalgenome.org'})">ClinGen Validity</a></dd>
<dd><a href="https://medlineplus.gov/genetics/gene/gjb6" class="mim-tip-hint" title="Consumer-friendly information about the effects of genetic variation on human health." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MedlinePlus Genetics', 'domain': 'medlineplus.gov'})">MedlinePlus Genetics</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=604418[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Variation</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/clinvar?term=604418[MIM]" class="mim-tip-hint" title="ClinVar aggregates information about sequence variation and its relationship to human health." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ClinVar', 'domain': 'ncbi.nlm.nih.gov'})">ClinVar</a></dd>
<dd><a href="https://gnomad.broadinstitute.org/gene/ENSG00000121742" class="mim-tip-hint" title="The Genome Aggregation Database (gnomAD), Broad Institute." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'gnomAD', 'domain': 'gnomad.broadinstitute.org'})">gnomAD</a></dd>
<dd><a href="https://www.gwascentral.org/search?q=GJB6" class="mim-tip-hint" title="GWAS Central; summary level genotype-to-phenotype information from genetic association studies." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GWAS Central', 'domain': 'gwascentral.org'})">GWAS Central </a></dd>
<dd><a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=GJB6" class="mim-tip-hint" title="Human Gene Mutation Database; published mutations causing or associated with human inherited disease; disease-associated/functional polymorphisms." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'HGMD', 'domain': 'hgmd.cf.ac.uk'})">HGMD</a></dd>
<dd>Locus Specific DBs</dd>
<dd style="margin-left: 0.5em;"><a href="http://davinci.crg.es/deafness/" title="The Connexin-deafness homepage" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">The Connexin-deafness home…</a></dd><dd style="margin-left: 0.5em;"><a href="http://hereditaryhearingloss.org/" title="Hereditary Hearing Loss Homepage" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">Hereditary Hearing Loss Ho…</a></dd><dd style="margin-left: 0.5em;"><a href="https://research.cchmc.org/LOVD2/home.php?select_db=GJB6" title="CCHMC - Human Genetics Mutation Database" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">CCHMC - Human Genetics Mut…</a></dd>
<dd><a href="https://evs.gs.washington.edu/EVS/PopStatsServlet?searchBy=Gene+Hugo&target=GJB6&upstreamSize=0&downstreamSize=0&x=0&y=0" class="mim-tip-hint" title="National Heart, Lung, and Blood Institute Exome Variant Server." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NHLBI EVS', 'domain': 'evs.gs.washington.edu'})">NHLBI EVS</a></dd>
<dd><a href="https://www.pharmgkb.org/gene/PA28699" class="mim-tip-hint" title="Pharmacogenomics Knowledge Base; curated and annotated information regarding the effects of human genetic variations on drug response." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PharmGKB', 'domain': 'pharmgkb.org'})">PharmGKB</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Animal Models</dt>
<dd><a href="https://www.alliancegenome.org/gene/HGNC:4288" class="mim-tip-hint" title="Search Across Species; explore model organism and human comparative genomics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Alliance Genome', 'domain': 'alliancegenome.org'})">Alliance Genome</a></dd>
<dd><a href="https://www.mousephenotype.org/data/genes/MGI:107588" class="mim-tip-hint" title="International Mouse Phenotyping Consortium." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'IMPC', 'domain': 'knockoutmouse.org'})">IMPC</a></dd>
<dd><a href="http://v1.marrvel.org/search/gene/GJB6#HomologGenesPanel" class="mim-tip-hint" title="Model organism Aggregated Resources for Rare Variant ExpLoration." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MARRVEL', 'domain': 'marrvel.org'})">MARRVEL</a></dd>
<dd><a href="http://www.informatics.jax.org/marker/MGI:107588" class="mim-tip-hint" title="Mouse Genome Informatics; international database resource for the laboratory mouse, including integrated genetic, genomic, and biological data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MGI Mouse Gene', 'domain': 'informatics.jax.org'})">MGI Mouse Gene</a></dd>
<dd><a href="https://www.mmrrc.org/catalog/StrainCatalogSearchForm.php?search_query=MGI:107588" class="mim-tip-hint" title="Mutant Mouse Resource & Research Centers." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MMRRC', 'domain': 'mmrrc.org'})">MMRRC</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gene/10804/ortholog/" class="mim-tip-hint" title="Orthologous genes at NCBI." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Orthologs', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Orthologs</a></dd>
<dd><a href="https://www.orthodb.org/?ncbi=10804" class="mim-tip-hint" title="Hierarchical catalogue of orthologs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrthoDB', 'domain': 'orthodb.org'})">OrthoDB</a></dd>
<dd><a href="https://zfin.org/ZDB-GENE-040406-1" class="mim-tip-hint" title="The Zebrafish Model Organism Database." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ZFin', 'domain': 'zfin.org'})">ZFin</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Cellular Pathways</dt>
<dd><a href="https://reactome.org/content/query?q=GJB6&species=Homo+sapiens&types=Reaction&types=Pathway&cluster=true" class="definition" title="Protein-specific information in the context of relevant cellular pathways." target="_blank" onclick="gtag('event', 'mim_outbound', {{'name': 'Reactome', 'domain': 'reactome.org'}})">Reactome</a></dd>
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Search: <span class="mim-text-font">121011 601544 604418 612643 (Search in: MIM number)</span>
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Results: 4 entries.
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612643.
DEAFNESS, AUTOSOMAL DOMINANT 3B; DFNA3B
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Cytogenetic location:
<span class="mim-font">13q12.11</a></span>
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<span class="text-success">Matching terms: <span class="mim-font">612643</span></span>
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<span class="text-danger"><strong>#</strong></span>
601544.
DEAFNESS, AUTOSOMAL DOMINANT 3A; DFNA3A
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Cytogenetic location:
<span class="mim-font">13q12.11</a></span>
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<span class="text-success">Matching terms: <span class="mim-font">601544</span></span>
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121011.
GAP JUNCTION PROTEIN, BETA-2; GJB2
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Cytogenetic location: <span class="mim-font">13q12.11</span>,
Genomic coordinates <span class="small">(GRCh38)</span>: <span class="mim-font">13:20,187,470-20,192,938</span>
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<span class="text-danger"><strong>*</strong></span>
604418.
GAP JUNCTION PROTEIN, BETA-6; GJB6
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Cytogenetic location: <span class="mim-font">13q12.11</span>,
Genomic coordinates <span class="small">(GRCh38)</span>: <span class="mim-font">13:20,221,962-20,232,319</span>
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