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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://www.ebi.ac.uk/efo/EFO_0009081 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0009081">
        <rdfs:label>Heterotaxia</rdfs:label>
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    <!-- http://www.ebi.ac.uk/efo/EFO_0009136 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0009136">
        <rdfs:label>heterotaxy, visceral, x-linked</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.ebi.ac.uk/efo/EFO_0009081"/>
        <oboInOwl:hasDbXref>MONDO:0010607</oboInOwl:hasDbXref>
        <ns2:IAO_0000115>X-linked, right/left transposition of thoracic and/or abdominal organs. This condition is caused by mutations in the ZIC3 gene, is inherited in an X-linked recessive fashion , and is usually seen in males. Physical features include heart abnormalities such as dextrocardia , transposition of great vessels , ventricular septal defect , patent ductus arteriosus , pulmonic stenosis ; situs inversus, and missing (asplenia) and/or extra spleens (polysplenia).Affected individualscan also experience abnormalities in the development of the midline of the body, which can cause holoprosencephaly , myelomeningocele , urological anomalies, widely spaced eyes (hypertelorism), cleft palate , and abnormalities of the sacral spine and anus. Heterotaxia with recurrent respiratory infections are called primary ciliary dyskinesia .</ns2:IAO_0000115>
        <ns2:IAO_0000117>Hannah McLaren</ns2:IAO_0000117>
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