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    <!-- http://purl.obolibrary.org/obo/MONDO_0010319 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010319">
        <rdfs:label>syndromic X-linked intellectual disability Hedera type</rdfs:label>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5588</ns3:IAO_0000233>
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        <oboInOwl:hasDbXref>GARD:0016834</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>X-linked intellectual disability, Hedera type is a rare X-linked intellectual disability syndrome characterized by an onset in infancy of delayed motor and speech milestones, generalized tonic-clonic seizures and drop attacks, and mild to moderate intellectual disability. Additional, less common manifestations include scoliosis, ataxia (resulting in progressive gait disturbance), and bilateral pes planovalgus. Physical appearance is normal with no dysmorphic features reported.</ns3:IAO_0000115>
        <oboInOwl:id>MONDO:0010319</oboInOwl:id>
        <oboInOwl:hasExactSynonym>mental retardation, X-linked, syndromic, Hedera type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:93952</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>X-linked intellectual disability, Hedera type</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIM:300423</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1845543</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:337257</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>X-linked intellectual disability with epilepsy</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>DOID:0060806</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016160 -->

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        <rdfs:label>X-linked intellectual disability-epilepsy syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100146 -->

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        <rdfs:label>ATP6AP2-related disorder</rdfs:label>
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