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    <!-- http://purl.obolibrary.org/obo/MONDO_0000426 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000426">
        <rdfs:label>autosomal dominant disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0007318 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007318">
        <rdfs:label>Alagille syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016862 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016862">
        <rdfs:label>Alagille syndrome due to a JAG1 point mutation</rdfs:label>
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        <oboInOwl:hasExactSynonym>Alagille-Watson syndrome due to a JAG1 point mutation</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Alagille syndrome-JAG1</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Alagille syndrome due to a JAG1 point mutation</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:365434</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>GARD:0017251</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:118450</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:261619</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Alagille syndrome 1</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>UMLS:C1956125</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>syndromic bile duct paucity due to a JAG1 point mutation</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>arteriohepatic dysplasia due to a JAG1 point mutation</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Alagille syndrome type 1</oboInOwl:hasExactSynonym>
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        <rdfs:label>obsolete_Alagille syndrome due to a JAG1 point mutation</rdfs:label>
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