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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004003 -->

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        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#TransitiveProperty"/>
        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/mondo#disease_has_major_feature -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/mondo#disease_has_major_feature">
        <rdfs:label>disease has major feature</rdfs:label>
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    <!-- http://identifiers.org/hgnc/29099 -->

    <Class rdf:about="http://identifiers.org/hgnc/29099">
        <rdfs:label>TELO2</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000508 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000508">
        <rdfs:label>syndromic intellectual disability</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0002320 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002320">
        <rdfs:label>congenital nervous system disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005027 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005027">
        <rdfs:label>epilepsy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005328 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005328">
        <rdfs:label>eye disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0014848 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0014848">
        <rdfs:label>TELO2-related intellectual disability-neurodevelopmental disorder</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002320"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015159"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015160"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016908"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019054"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020022"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100545"/>
        <rdfs:subClassOf>
            <Restriction>
                <onProperty rdf:resource="http://purl.obolibrary.org/obo/mondo#disease_has_major_feature"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020022"/>
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                <someValuesFrom rdf:resource="http://identifiers.org/hgnc/29099"/>
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        </rdfs:subClassOf>
        <ns6:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5588</ns6:IAO_0000233>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/you_hoover_fong_syndrome</ns3:curated_content_resource>
        <oboInOwl:hasRelatedSynonym>YHFS</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0017898</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0014848</oboInOwl:id>
        <oboInOwl:hasDbXref>OMIM:616954</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:934745</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:488642</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C4310778</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>you-Hoover-Fong syndrome</oboInOwl:hasExactSynonym>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/934745"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C4310778"/>
        <ns3:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000508"/>
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        <ns3:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005328"/>
        <ns3:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015368"/>
        <ns3:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015620"/>
        <ns3:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020215"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_488642"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/616954"/>
        <ns3:curated_content_resource rdf:resource="https://search.clinicalgenome.org/kb/conditions/MONDO:0014848"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015159 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015159">
        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-intellectual disability</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015160 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015160">
        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015368 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015368">
        <rdfs:label>obsolete neuro-ophthalmological disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015620 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015620">
        <rdfs:label>obsolete syndromic urogenital tract malformation</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016908 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016908">
        <rdfs:label>partial monosomy of the long arm of chromosome 9</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019054 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019054">
        <rdfs:label>congenital limb malformation</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020022 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020022">
        <rdfs:label>central nervous system malformation</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020215 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020215">
        <rdfs:label>obsolete syndromic corneal dystrophy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020240 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020240">
        <rdfs:label>obsolete syndromic retinitis pigmentosa</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0100545 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100545">
        <rdfs:label>hereditary neurological disease</rdfs:label>
    </Class>
</rdf:RDF>



<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



