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    <!-- http://purl.obolibrary.org/obo/HP_0000005 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0000005">
        <rdfs:label>Mode of Inheritance</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0000006 -->

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        <rdfs:label>Autosomal Dominant</rdfs:label>
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        <oboInOwl:hasExactSynonym>Autosomal Dominant Inheritance</oboInOwl:hasExactSynonym>
        <ns2:IAO_0000115>A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.</ns2:IAO_0000115>
        <oboInOwl:hasExactSynonym>Autosomal Dominant Predisposition</oboInOwl:hasExactSynonym>
        <ns2:SCDO_1000288>Sufficient</ns2:SCDO_1000288>
        <oboInOwl:hasExactSynonym>Autosomal Dominant Form</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>HP:0000006</oboInOwl:hasDbXref>
        <ns2:SCDO_1000910>SCDO:1000140</ns2:SCDO_1000910>
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