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    <!-- http://purl.obolibrary.org/obo/RO_0004003 -->

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        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/6250 -->

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        <oboInOwl:hasDbXref>MEDGEN:1639277</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Any Zimmermann-Laband syndrome in which the cause of the disease is a mutation in the KCNH1 gene.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:0015071</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Laband Syndrome</oboInOwl:hasExactSynonym>
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