nih-gov/www.ncbi.nlm.nih.gov/omim/608895

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Entry
- #608895 - MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3
- OMIM
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<span class="h4">#608895</span>
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<a href="#title"><strong>Title</strong></a>
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<a href="#phenotypeMap"><strong>Phenotype-Gene Relationships</strong></a>
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<a href="/clinicalSynopsis/608895"><strong>Clinical Synopsis</strong></a>
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<a href="/phenotypicSeries/PS603075"> <strong>Phenotypic Series</strong> </a>
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<a href="#text"><strong>Text</strong></a>
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<a href="#description">Description</a>
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<a href="#clinicalFeatures">Clinical Features</a>
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<a href="#pathogenesis">Pathogenesis</a>
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<a href="#molecularGenetics">Molecular Genetics</a>
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<a href="#references"><strong>References</strong></a>
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<a href="#contributors"><strong>Contributors</strong></a>
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</span>
</div>
<div id="mimClinicalResourcesLinksFold" class="panel-collapse collapse in mimLinksFold" role="tabpanel" aria-labelledby="clinicalResources">
<div class="panel-body small mim-panel-body">
<div><a href="https://clinicaltrials.gov/search?cond=(MACULAR DEGENERATION, AGE-RELATED) OR (FBLN5)" class="mim-tip-hint" title="Clinical Trials" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Clinical Trials', 'domain': 'clinicaltrials.gov'})">Clinical Trials</a></div>
<div><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=20480&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></div>
<div><a href="https://www.diseaseinfosearch.org/x/7653" class="mim-tip-hint" title="Network of disease-specific advocacy organizations, universities, private companies, government agencies, and public policy organizations." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Genetic Alliance', 'domain': 'diseaseinfosearch.org'})">Genetic Alliance</a></div>
<div><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=608895[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></div>
<div><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=280598" class="mim-tip-hint" title="European reference portal for information on rare diseases and orphan drugs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">OrphaNet</a></div>
</div>
</div>
</div>
</div>
</div>
</div>
<span>
<span class="mim-tip-bottom" qtip_title="<strong>Looking for this gene or this phenotype in other resources?</strong>" qtip_text="Select a related resource from the dropdown menu and click for a targeted link to information directly relevant.">
&nbsp;
</span>
</span>
</div>
<div class="col-lg-8 col-lg-pull-2 col-md-8 col-md-pull-2 col-sm-8 col-sm-pull-2 col-xs-12">
<div>
<a id="title" class="mim-anchor"></a>
<div>
<a id="number" class="mim-anchor"></a>
<div class="text-right">
<a href="#" class="mim-tip-icd" qtip_title="<strong>ICD+</strong>" qtip_text="
<strong>ORPHA:</strong> 280598<br />
">ICD+</a>
</div>
<div>
<span class="h3">
<span class="mim-font mim-tip-hint" title="Phenotype description, molecular basis known">
<span class="text-danger"><strong>#</strong></span>
608895
</span>
</span>
</div>
</div>
<div>
<a id="preferredTitle" class="mim-anchor"></a>
<h3>
<span class="mim-font">
MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3
</span>
</h3>
</div>
<div>
<br />
</div>
</div>
<div>
<a id="phenotypeMap" class="mim-anchor"></a>
<h4>
<span class="mim-font">
<strong>Phenotype-Gene Relationships</strong>
</span>
</h4>
<div>
<table class="table table-bordered table-condensed table-hover small mim-table-padding">
<thead>
<tr class="active">
<th>
Location
</th>
<th>
Phenotype
</th>
<th>
Phenotype <br /> MIM number
</th>
<th>
Inheritance
</th>
<th>
Phenotype <br /> mapping key
</th>
<th>
Gene/Locus
</th>
<th>
Gene/Locus <br /> MIM number
</th>
</tr>
</thead>
<tbody>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/464?start=-3&limit=10&highlight=464">
14q32.12
</a>
</span>
</td>
<td>
<span class="mim-font">
Macular degeneration, age-related, 3
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608895"> 608895 </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">
FBLN5
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604580"> 604580 </a>
</span>
</td>
</tr>
</tbody>
</table>
</div>
</div>
<div>
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<a href="/clinicalSynopsis/608895" class="btn btn-warning" role="button"> Clinical Synopsis </a>
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<a href="/phenotypicSeries/PS603075" class="btn btn-info" role="button"> Phenotypic Series </a>
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<button type="button" class="btn btn-success dropdown-toggle" data-toggle="dropdown" aria-haspopup="true" aria-expanded="false">
PheneGene Graphics <span class="caret"></span>
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<ul class="dropdown-menu" style="width: 17em;">
<li><a href="/graph/linear/608895" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Linear'})"> Linear </a></li>
<li><a href="/graph/radial/608895" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Radial'})"> Radial </a></li>
</ul>
</div>
<span class="glyphicon glyphicon-question-sign mim-tip-hint" title="OMIM PheneGene graphics depict relationships between phenotypes, groups of related phenotypes (Phenotypic Series), and genes.<br /><a href='/static/omim/pdf/OMIM_Graphics.pdf' target='_blank'>A quick reference overview and guide (PDF)</a>"></span>
<div>
<p />
</div>
<div id="mimClinicalSynopsisFold" class="well well-sm collapse mimSingletonToggleFold">
<div class="small" style="margin: 5px">
<div>
<div>
<span class="h5 mim-font">
<strong> INHERITANCE </strong>
</span>
</div>
<div style="margin-left: 2em;">
<div>
<span class="mim-font">
- Autosomal dominant <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/263681008" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">263681008</a>, <a href="https://purl.bioontology.org/ontology/SNOMEDCT/771269000" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">771269000</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0443147&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0443147</a>, <a href="https://bioportal.bioontology.org/search?q=C1867440&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C1867440</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000006" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000006</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0000006" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0000006</a>]</span><br />
</span>
</div>
</div>
</div>
<div>
<div>
<span class="h5 mim-font">
<strong> HEAD & NECK </strong>
</span>
</div>
<div style="margin-left: 2em;">
<div>
<div>
<span class="h5 mim-font">
<em> Eyes </em>
</span>
</div>
<div style="margin-left: 2em;">
<span class="mim-font">
- Reduced visual acuity <span class="mim-feature-ids hidden">[SNOMEDCT: <a href="https://purl.bioontology.org/ontology/SNOMEDCT/13164000" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'SNOMEDCT\', \'domain\': \'bioontology.org\'})">13164000</a>]</span> <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0234632&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0234632</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0007663" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0007663</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0007663" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0007663</a>]</span><br /> -
Numerous uniformly small round yellow drusen at temporal edge of macula <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C5678058&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C5678058</a>]</span><br /> -
Macular retinal detachment <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C5678059&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C5678059</a>]</span><br /> -
Choroidal neovascularization (in some patients) <span class="mim-feature-ids hidden">[UMLS: <a href="https://bioportal.bioontology.org/search?q=C0600518&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C0600518</a>, <a href="https://bioportal.bioontology.org/search?q=C5574745&searchproperties=true" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'UMLS\', \'domain\': \'bioontology.org\'})">C5574745</a> HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0011506" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0011506</a>]</span> <span class="mim-feature-ids hidden">[HPO: <a href="https://hpo.jax.org/app/browse/term/HP:0011506" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'HPO\', \'domain\': \'hpo.jax.org\'})">HP:0011506</a>]</span><br />
</span>
</div>
</div>
</div>
</div>
<div>
<div>
<span class="h5 mim-font">
<strong> MISCELLANEOUS </strong>
</span>
</div>
<div style="margin-left: 2em;">
<div>
<span class="mim-font">
- Onset generally after the age of 50<br />
</span>
</div>
</div>
</div>
<div>
<div>
<span class="h5 mim-font">
<strong> MOLECULAR BASIS </strong>
</span>
</div>
<div style="margin-left: 2em;">
<div>
<span class="mim-font">
- Caused by mutation in the fibulin 5 gene (FBLN5, <a href="/entry/604580#0003">604580.0003</a>)<br />
</span>
</div>
</div>
</div>
<div class="text-right">
<a href="#mimClinicalSynopsisFold" data-toggle="collapse">&#9650;&nbsp;Close</a>
</div>
</div>
</div>
<div id="mimPhenotypicSeriesFold" 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>
Macular degeneration, age-related
- <a href="/phenotypicSeries/PS603075">PS603075</a>
- 20 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/1/814?start=-3&limit=10&highlight=814"> 1p22.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/153800"> {Macular degeneration, age-related, 2} </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/153800"> 153800 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601691"> ABCA4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601691"> 601691 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1502?start=-3&limit=10&highlight=1502"> 1q25.3-q31.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603075"> {Macular degeneration, age-related, 1} </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/603075"> 603075 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608548"> HMCN1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608548"> 608548 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1528?start=-3&limit=10&highlight=1528"> 1q31.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610698"> {Macular degeneration, age-related, 4} </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/610698"> 610698 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/134370"> CFH </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/134370"> 134370 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1529?start=-3&limit=10&highlight=1529"> 1q31.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603075"> {Macular degeneration, age-related, reduced risk of} </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/603075"> 603075 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605336"> CFHR3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605336"> 605336 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1530?start=-3&limit=10&highlight=1530"> 1q31.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603075"> {Macular degeneration, age-related, reduced risk of} </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/603075"> 603075 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/134371"> CFHR1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/134371"> 134371 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/189?start=-3&limit=10&highlight=189"> 3p22.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613784"> {Macular degeneration, age-related, 12} </a>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613784"> 613784 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601470"> CX3CR1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601470"> 601470 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/482?start=-3&limit=10&highlight=482"> 4q25 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615439"> {Macular degeneration, age-related, 13, susceptibility to} </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/615439"> 615439 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/217030"> CFI </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/217030"> 217030 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/126?start=-3&limit=10&highlight=126"> 5p13.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615591"> {Macular degeneration, age-related, 15, susceptibility to} </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/615591"> 615591 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120940"> C9 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120940"> 120940 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/342?start=-3&limit=10&highlight=342"> 6p21.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615489"> {Macular degeneration, age-related, 14, reduced risk of} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Digenic dominant">DD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615489"> 615489 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613927"> C2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613927"> 613927 </a>
</span>
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<span class="mim-font">
<a href="/geneMap/6/343?start=-3&limit=10&highlight=343"> 6p21.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615489"> {Macular degeneration, age-related, 14, reduced risk of} </a>
</span>
</td>
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<span class="mim-font">
<abbr class="mim-tip-hint" title="Digenic dominant">DD</abbr>
</span>
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<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
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<span class="mim-font">
<a href="/entry/615489"> 615489 </a>
</span>
</td>
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<span class="mim-font">
<a href="/entry/138470"> CFB </a>
</span>
</td>
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<span class="mim-font">
<a href="/entry/138470"> 138470 </a>
</span>
</td>
</tr>
<tr>
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<span class="mim-font">
<a href="/geneMap/9/416?start=-3&limit=10&highlight=416"> 9q32-q33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611488"> Macular degeneration, age-related, 10 </a>
</span>
</td>
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<span class="mim-font">
</span>
</td>
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<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
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<span class="mim-font">
<a href="/entry/611488"> 611488 </a>
</span>
</td>
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<span class="mim-font">
<a href="/entry/611488"> ARMD10 </a>
</span>
</td>
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<span class="mim-font">
<a href="/entry/611488"> 611488 </a>
</span>
</td>
</tr>
<tr>
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<span class="mim-font">
<a href="/geneMap/10/190?start=-3&limit=10&highlight=190"> 10q11.23 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613761"> {Macular degeneration, age-related, susceptibility to, 5} </a>
</span>
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<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
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<span class="mim-font">
<a href="/entry/613761"> 613761 </a>
</span>
</td>
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<span class="mim-font">
<a href="/entry/609413"> ERCC6 </a>
</span>
</td>
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<span class="mim-font">
<a href="/entry/609413"> 609413 </a>
</span>
</td>
</tr>
<tr>
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<span class="mim-font">
<a href="/geneMap/10/623?start=-3&limit=10&highlight=623"> 10q26.13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613778"> {Macular degeneration, age-related, 8} </a>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
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<span class="mim-font">
<a href="/entry/613778"> 613778 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611313"> LOC387715 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611313"> 611313 </a>
</span>
</td>
</tr>
<tr>
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<span class="mim-font">
<a href="/geneMap/10/624?start=-3&limit=10&highlight=624"> 10q26.13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610149"> {Macular degeneration, age-related, neovascular type} </a>
</span>
</td>
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<span class="mim-font">
</span>
</td>
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<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610149"> 610149 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602194"> HTRA1 </a>
</span>
</td>
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<span class="mim-font">
<a href="/entry/602194"> 602194 </a>
</span>
</td>
</tr>
<tr>
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<span class="mim-font">
<a href="/geneMap/10/624?start=-3&limit=10&highlight=624"> 10q26.13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610149"> {Macular degeneration, age-related, 7} </a>
</span>
</td>
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<span class="mim-font">
</span>
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<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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</td>
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<span class="mim-font">
<a href="/entry/610149"> 610149 </a>
</span>
</td>
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<span class="mim-font">
<a href="/entry/602194"> HTRA1 </a>
</span>
</td>
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<span class="mim-font">
<a href="/entry/602194"> 602194 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/464?start=-3&limit=10&highlight=464"> 14q32.12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608895"> Macular degeneration, age-related, 3 </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>
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<span class="mim-font">
<a href="/entry/608895"> 608895 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604580"> FBLN5 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604580"> 604580 </a>
</span>
</td>
</tr>
<tr>
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<span class="mim-font">
<a href="/geneMap/19/117?start=-3&limit=10&highlight=117"> 19p13.3 </a>
</span>
</td>
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<span class="mim-font">
<a href="/entry/613757"> ?Macular degeneration, age-related, 6 </a>
</span>
</td>
<td>
<span class="mim-font">
</span>
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<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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</td>
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<span class="mim-font">
<a href="/entry/613757"> 613757 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610362"> RAX2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610362"> 610362 </a>
</span>
</td>
</tr>
<tr>
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<span class="mim-font">
<a href="/geneMap/19/189?start=-3&limit=10&highlight=189"> 19p13.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611378"> {Macular degeneration, age-related, 9} </a>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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<span class="mim-font">
<a href="/entry/611378"> 611378 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120700"> C3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120700"> 120700 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/19/803?start=-3&limit=10&highlight=803"> 19q13.32 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603075"> {?Macular degeneration, age-related} </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>
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<span class="mim-font">
<a href="/entry/603075"> 603075 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/107741"> APOE </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/107741"> 107741 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/20/154?start=-3&limit=10&highlight=154"> 20p11.21 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611953"> {Macular degeneration, age-related, 11} </a>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611953"> 611953 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604312"> CST3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604312"> 604312 </a>
</span>
</td>
</tr>
</tbody>
</table>
</div>
<div class="text-right small">
<a href="#mimPhenotypicSeriesFold" data-toggle="collapse">&#9650;&nbsp;Close</a>
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</div>
<div>
<br />
</div>
<div>
<a id="text" class="mim-anchor"></a>
<h4 href="#mimTextFold" id="mimTextToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
<span id="mimTextToggleTriangle" class="small mimTextToggleTriangle">&#9660;</span>
<span class="mim-font">
<span class="mim-tip-floating" qtip_title="<strong>Looking For More References?</strong>" qtip_text="Click the 'reference plus' icon &lt;span class='glyphicon glyphicon-plus-sign'&gt;&lt;/span&gt at the end of each OMIM text paragraph to see more references related to the content of the preceding paragraph.">
<strong>TEXT</strong>
</span>
</span>
</h4>
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<span class="mim-text-font">
<p>A number sign (#) is used with this entry because of evidence that age-related macular degeneration-3 (ARMD3) is caused by heterozygous mutation in the gene encoding fibulin-5 (FBLN5; <a href="/entry/604580">604580</a>) on chromosome 14q32.</p><p>Heterozygous mutation in the FBLN5 gene can also cause autosomal dominant cutis laxa-2 (ADCL2; <a href="/entry/614434">614434</a>) and demyelinating Charcot-Marie-Tooth disease type 1H (CMT1H; <a href="/entry/619764">619764</a>).</p>
</span>
<div>
<br />
</div>
</div>
<div>
<a id="description" class="mim-anchor"></a>
<h4 href="#mimDescriptionFold" id="mimDescriptionToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
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<span class="mim-font">
<strong>Description</strong>
</span>
</h4>
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<div id="mimDescriptionFold" class="collapse in ">
<span class="mim-text-font">
<p>Age-related macular degeneration-3 (ARMD3) is characterized by numerous small round yellow lesions visible at the temporal edge of the macula. Larger, less distinct yellow areas near the center of the macula are also observed, which represent areas of pigment epithelial detachment (<a href="#2" class="mim-tip-reference" title="Stone, E. M., Braun, T. A., Russell, S. R., Kuehn, M. H., Lotery, A. J., Moore, P. A., Eastman, C. G., Casavant, T. L., Sheffield, V. C. &lt;strong&gt;Missense variations in the fibulin 5 gene and age-related macular degeneration.&lt;/strong&gt; New Eng. J. Med. 351: 346-353, 2004.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/15269314/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;15269314&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1056/NEJMoa040833&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="15269314">Stone et al., 2004</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=15269314" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>For a phenotypic description and a discussion of genetic heterogeneity of age-related macular degeneration, see <a href="/entry/603075">603075</a>.</p>
</span>
<div>
<br />
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</div>
<div>
<a id="clinicalFeatures" class="mim-anchor"></a>
<h4 href="#mimClinicalFeaturesFold" id="mimClinicalFeaturesToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
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<strong>Clinical Features</strong>
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<div id="mimClinicalFeaturesFold" class="collapse in mimTextToggleFold">
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<p><a href="#2" class="mim-tip-reference" title="Stone, E. M., Braun, T. A., Russell, S. R., Kuehn, M. H., Lotery, A. J., Moore, P. A., Eastman, C. G., Casavant, T. L., Sheffield, V. C. &lt;strong&gt;Missense variations in the fibulin 5 gene and age-related macular degeneration.&lt;/strong&gt; New Eng. J. Med. 351: 346-353, 2004.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/15269314/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;15269314&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1056/NEJMoa040833&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="15269314">Stone et al. (2004)</a> identified 7 unrelated patients with age-related macular degeneration and mutations in the FBLN5 gene. Upon examination in a retina clinic, all 7 patients showed clusters of small, round, uniform drusen in association with variable degrees of detachment of retinal pigment epithelium. Fluorescein angiography revealed that the small dot-like lesions were brightly hyperfluorescent, whereas the areas of retinal detachment were much less visible. Three of the patients also showed evidence of choroidal neovascularization. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=15269314" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
</span>
<div>
<br />
</div>
</div>
<div>
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<strong>Pathogenesis</strong>
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<p><a href="#1" class="mim-tip-reference" title="Mullins, R. F., Olvera, M. A., Clark, A. F., Stone, E. M. &lt;strong&gt;Fibulin-5 distribution in human eyes: relevance to age-related macular degeneration.&lt;/strong&gt; Exp. Eye Res. 84: 378-380, 2007.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/17109857/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;17109857&lt;/a&gt;, &lt;a href=&quot;https://www.ncbi.nlm.nih.gov/pmc/?term=17109857[PMID]&amp;report=imagesdocsum&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed Image&#x27;, &#x27;domain&#x27;: &#x27;ncbi.nlm.nih.gov&#x27;})&quot;&gt;images&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1016/j.exer.2006.09.021&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="17109857">Mullins et al. (2007)</a> localized the fibulin-5 protein to the Bruch membrane and to the intercapillary pillars of the choriocapillaris in normal human donor eyes. In eyes with age-related macular degeneration, they localized the protein to pathologic basal deposits beneath the retinal pigment epithelium (RPE) as well as in some small drusen. <a href="#1" class="mim-tip-reference" title="Mullins, R. F., Olvera, M. A., Clark, A. F., Stone, E. M. &lt;strong&gt;Fibulin-5 distribution in human eyes: relevance to age-related macular degeneration.&lt;/strong&gt; Exp. Eye Res. 84: 378-380, 2007.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/17109857/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;17109857&lt;/a&gt;, &lt;a href=&quot;https://www.ncbi.nlm.nih.gov/pmc/?term=17109857[PMID]&amp;report=imagesdocsum&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed Image&#x27;, &#x27;domain&#x27;: &#x27;ncbi.nlm.nih.gov&#x27;})&quot;&gt;images&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1016/j.exer.2006.09.021&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="17109857">Mullins et al. (2007)</a> suggested that fibulin-5 may promote extracellular deposit formation in macular degeneration. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=17109857" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
</span>
<div>
<br />
</div>
</div>
<div>
<a id="molecularGenetics" class="mim-anchor"></a>
<h4 href="#mimMolecularGeneticsFold" id="mimMolecularGeneticsToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
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<strong>Molecular Genetics</strong>
</span>
</h4>
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<div id="mimMolecularGeneticsFold" class="collapse in mimTextToggleFold">
<span class="mim-text-font">
<p><a href="#2" class="mim-tip-reference" title="Stone, E. M., Braun, T. A., Russell, S. R., Kuehn, M. H., Lotery, A. J., Moore, P. A., Eastman, C. G., Casavant, T. L., Sheffield, V. C. &lt;strong&gt;Missense variations in the fibulin 5 gene and age-related macular degeneration.&lt;/strong&gt; New Eng. J. Med. 351: 346-353, 2004.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/15269314/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;15269314&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1056/NEJMoa040833&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="15269314">Stone et al. (2004)</a> studied 402 patients with age-related macular degeneration and identified 7 different mutations in the FBLN5 gene (<a href="/entry/604580#0003">604580.0003</a>-<a href="/entry/604580#0009">604580.0009</a>) that were not found in 429 controls (p = 0.006). <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=15269314" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<br />
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<div>
<a id="references"class="mim-anchor"></a>
<h4 href="#mimReferencesFold" id="mimReferencesToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
<span class="mim-font">
<span id="mimReferencesToggleTriangle" class="small mimTextToggleTriangle">&#9660;</span>
<strong>REFERENCES</strong>
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</h4>
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<p />
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<div id="mimReferencesFold" class="collapse in mimTextToggleFold">
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<a id="1" class="mim-anchor"></a>
<a id="Mullins2007" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Mullins, R. F., Olvera, M. A., Clark, A. F., Stone, E. M.
<strong>Fibulin-5 distribution in human eyes: relevance to age-related macular degeneration.</strong>
Exp. Eye Res. 84: 378-380, 2007.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/17109857/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">17109857</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/?term=17109857[PMID]&report=imagesdocsum" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Image', 'domain': 'ncbi.nlm.nih.gov'})">images</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=17109857" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1016/j.exer.2006.09.021" target="_blank">Full Text</a>]
</p>
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</li>
<li>
<a id="2" class="mim-anchor"></a>
<a id="Stone2004" class="mim-anchor"></a>
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Stone, E. M., Braun, T. A., Russell, S. R., Kuehn, M. H., Lotery, A. J., Moore, P. A., Eastman, C. G., Casavant, T. L., Sheffield, V. C.
<strong>Missense variations in the fibulin 5 gene and age-related macular degeneration.</strong>
New Eng. J. Med. 351: 346-353, 2004.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/15269314/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">15269314</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=15269314" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1056/NEJMoa040833" target="_blank">Full Text</a>]
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<a id="contributors" class="mim-anchor"></a>
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<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
Marla J. F. O'Neill - updated : 03/18/2022
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<div class="row collapse" id="mimCollapseContributors">
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<span class="mim-text-font">
Cassandra L. Kniffin - updated : 12/10/2015<br>Jane Kelly - updated : 7/9/2008
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<a id="creationDate" class="mim-anchor"></a>
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Creation Date:
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Marla J. F. O&#x27;Neill : 9/1/2004
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alopez : 03/18/2022
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carol : 03/03/2022<br>alopez : 03/02/2022<br>ckniffin : 02/24/2022<br>carol : 02/28/2017<br>carol : 02/28/2017<br>carol : 06/22/2016<br>carol : 12/21/2015<br>carol : 12/21/2015<br>ckniffin : 12/21/2015<br>carol : 12/21/2015<br>ckniffin : 12/10/2015<br>carol : 2/2/2010<br>carol : 7/9/2008<br>carol : 10/16/2007<br>wwang : 8/27/2007<br>alopez : 1/12/2007<br>carol : 9/2/2004
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<h3>
<span class="mim-font">
<strong>#</strong> 608895
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<h3>
<span class="mim-font">
MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3
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<span class="mim-text-font">
<strong>ORPHA:</strong> 280598; &nbsp;
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<h4>
<span class="mim-font">
<strong>Phenotype-Gene Relationships</strong>
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<table class="table table-bordered table-condensed small mim-table-padding">
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<th>
Location
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Phenotype
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Phenotype <br /> MIM number
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<th>
Inheritance
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<th>
Phenotype <br /> mapping key
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Gene/Locus
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Gene/Locus <br /> MIM number
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<span class="mim-font">
14q32.12
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Macular degeneration, age-related, 3
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<span class="mim-font">
608895
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Autosomal dominant
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3
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FBLN5
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604580
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<strong>TEXT</strong>
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<p>A number sign (#) is used with this entry because of evidence that age-related macular degeneration-3 (ARMD3) is caused by heterozygous mutation in the gene encoding fibulin-5 (FBLN5; 604580) on chromosome 14q32.</p><p>Heterozygous mutation in the FBLN5 gene can also cause autosomal dominant cutis laxa-2 (ADCL2; 614434) and demyelinating Charcot-Marie-Tooth disease type 1H (CMT1H; 619764).</p>
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<strong>Description</strong>
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<p>Age-related macular degeneration-3 (ARMD3) is characterized by numerous small round yellow lesions visible at the temporal edge of the macula. Larger, less distinct yellow areas near the center of the macula are also observed, which represent areas of pigment epithelial detachment (Stone et al., 2004). </p><p>For a phenotypic description and a discussion of genetic heterogeneity of age-related macular degeneration, see 603075.</p>
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<strong>Clinical Features</strong>
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<p>Stone et al. (2004) identified 7 unrelated patients with age-related macular degeneration and mutations in the FBLN5 gene. Upon examination in a retina clinic, all 7 patients showed clusters of small, round, uniform drusen in association with variable degrees of detachment of retinal pigment epithelium. Fluorescein angiography revealed that the small dot-like lesions were brightly hyperfluorescent, whereas the areas of retinal detachment were much less visible. Three of the patients also showed evidence of choroidal neovascularization. </p>
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<strong>Pathogenesis</strong>
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</h4>
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<span class="mim-text-font">
<p>Mullins et al. (2007) localized the fibulin-5 protein to the Bruch membrane and to the intercapillary pillars of the choriocapillaris in normal human donor eyes. In eyes with age-related macular degeneration, they localized the protein to pathologic basal deposits beneath the retinal pigment epithelium (RPE) as well as in some small drusen. Mullins et al. (2007) suggested that fibulin-5 may promote extracellular deposit formation in macular degeneration. </p>
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<h4>
<span class="mim-font">
<strong>Molecular Genetics</strong>
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</h4>
</div>
<span class="mim-text-font">
<p>Stone et al. (2004) studied 402 patients with age-related macular degeneration and identified 7 different mutations in the FBLN5 gene (604580.0003-604580.0009) that were not found in 429 controls (p = 0.006). </p>
</span>
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<h4>
<span class="mim-font">
<strong>REFERENCES</strong>
</span>
</h4>
<div>
<p />
</div>
<div>
<ol>
<li>
<p class="mim-text-font">
Mullins, R. F., Olvera, M. A., Clark, A. F., Stone, E. M.
<strong>Fibulin-5 distribution in human eyes: relevance to age-related macular degeneration.</strong>
Exp. Eye Res. 84: 378-380, 2007.
[PubMed: 17109857]
[Full Text: https://doi.org/10.1016/j.exer.2006.09.021]
</p>
</li>
<li>
<p class="mim-text-font">
Stone, E. M., Braun, T. A., Russell, S. R., Kuehn, M. H., Lotery, A. J., Moore, P. A., Eastman, C. G., Casavant, T. L., Sheffield, V. C.
<strong>Missense variations in the fibulin 5 gene and age-related macular degeneration.</strong>
New Eng. J. Med. 351: 346-353, 2004.
[PubMed: 15269314]
[Full Text: https://doi.org/10.1056/NEJMoa040833]
</p>
</li>
</ol>
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<span class="text-nowrap mim-text-font">
Contributors:
</span>
</div>
<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
Marla J. F. O&#x27;Neill - updated : 03/18/2022<br>Cassandra L. Kniffin - updated : 12/10/2015<br>Jane Kelly - updated : 7/9/2008
</span>
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</div>
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<div>
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<div class="col-lg-1 col-md-1 col-sm-2 col-xs-2">
<span class="text-nowrap mim-text-font">
Creation Date:
</span>
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<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
Marla J. F. O&#x27;Neill : 9/1/2004
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alopez : 03/18/2022<br>carol : 03/03/2022<br>alopez : 03/02/2022<br>ckniffin : 02/24/2022<br>carol : 02/28/2017<br>carol : 02/28/2017<br>carol : 06/22/2016<br>carol : 12/21/2015<br>carol : 12/21/2015<br>ckniffin : 12/21/2015<br>carol : 12/21/2015<br>ckniffin : 12/10/2015<br>carol : 2/2/2010<br>carol : 7/9/2008<br>carol : 10/16/2007<br>wwang : 8/27/2007<br>alopez : 1/12/2007<br>carol : 9/2/2004
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