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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002254">
        <rdfs:label>syndromic disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005039 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005039">
        <rdfs:label>reproductive system disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0007795 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007795">
        <rdfs:label>mullerian duct anomalies-limb anomalies syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6753</ns3:IAO_0000233>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/hypomelia_with_mullerian_duct_anomalies</ns4:curated_content_resource>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/mullerian_duct_anomalies_limb_anomalies_syndrome_2</ns4:curated_content_resource>
        <oboInOwl:hasRelatedSynonym>limb uterus syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C1840335</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Mullerian duct anomalies-limb anomalies syndrome is characterized by the association of mullerian duct and distal limb anomalies. It has been described in five individuals from one family. Females presented with anomalies ranging from a vaginal septum to complete duplication of uterus and vagina, and males presented with micropenis. The limb anomalies varied from postaxial polydactyly to severe upper limb hypoplasia with split hand. The mode of transmission is autosomal dominant.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>OMIM:146160</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2491</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>severe upper limb hypoplasia and Mullerian duct anomalies</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>hypomelia mullerian duct anomalies</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0002908</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007795</oboInOwl:id>
        <oboInOwl:hasDbXref>MEDGEN:327078</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C537155</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/327078"/>
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        <skos:exactMatch rdf:resource="https://omim.org/entry/146160"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015161 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015161">
        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome without intellectual disability</rdfs:label>
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