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        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/4214 -->

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        <rdfs:label>GDF1</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008832 -->

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        <rdfs:label>right atrial isomerism</rdfs:label>
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        <ns4:IAO_0000589>right atrial isomerism (disease)</ns4:IAO_0000589>
        <oboInOwl:hasDbXref>MEDGEN:465274</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>heterotaxy, Visceroatrial, autosomal recessive</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>bilateral right-sidedness sequence</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>splenic agenesis syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>asplenia with cardiovascular anomalies</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10068335</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Ivemark syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>asplenia syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Ivemark Syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>RAI</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C3178806</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>right isomerism</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>DOID:0060856</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>right atrial isomerism (ivemark)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0006795</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>polysplenia syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0008832</oboInOwl:id>
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        <oboInOwl:hasDbXref>OMIM:208530</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1305</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>right atrial isomerism (disease)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>HP:0011536</oboInOwl:hasDbXref>
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        <rdfs:label>visceral heterotaxy</rdfs:label>
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