<?xml version="1.0"?>
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     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
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    <!-- 
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000412"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008843 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0008843">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015620"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015650"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019589"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019721"/>
        <ns2:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome is characterised by sensorineural deafness, diabetes mellitus, progressive neurological deterioration with photomyoclonic epilepsy, and progressive nephropathy. It has been described in two brothers. Premature atherosclerosis of renal, coronary, and cerebral arteries and the aorta was also observed.</ns2:IAO_0000115>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Feigenbaum Bergeron Richardson syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Feigenbaum-Bergeron-Richardson syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">GARD:0002279</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">MESH:C565928</oboInOwl:hasDbXref>
        <oboInOwl:id rdf:datatype="http://www.w3.org/2001/XMLSchema#string">MONDO:0008843</oboInOwl:id>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">OMIM:209010</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Orphanet:1192</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">SCTID:720519003</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus, photomyoclonus, and degenerative neurologic disease</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">premature atherosclerosis with photomyoclonic epilepsy, deafness, diabetes mellitus, nephropathy, and neurodegenerative disorder</oboInOwl:hasRelatedSynonym>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C565928"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/omim/209010"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/720519003"/>
        <skos:closeMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C1859596"/>
        <skos:closeMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C2931125"/>
        <oboInOwl:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_malformation_syndrome"/>
        <ns2:IAO_0000412 rdf:resource="http://purl.obolibrary.org/obo/mondo.owl"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_1192"/>
    </Class>
    


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

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015620">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">syndromic urogenital tract malformation</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015650 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015650">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">epilepsy syndrome</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019589 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019589">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">syndromic genetic deafness</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019721 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019721">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">syndromic renal or urinary tract malformation</rdfs:label>
    </Class>
</rdf:RDF>



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



