<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/EFO?iri=http://purl.obolibrary.org/obo/MONDO_0019262"?>
<rdf:RDF xmlns="http://www.w3.org/2002/07/owl#"
     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
     xmlns:owl="http://www.w3.org/2002/07/owl#"
     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
     xmlns:xsd="http://www.w3.org/2001/XMLSchema#"
     xmlns:skos="http://www.w3.org/2004/02/skos/core#"
     xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#"
     xmlns:ns2="http://purl.obolibrary.org/obo/mondo#"
     xmlns:ns4="http://purl.obolibrary.org/obo/"
     xmlns:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/">
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Annotation properties
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#excluded_subClassOf"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#closeMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#exactMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Datatypes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- 
    ///////////////////////////////////////////////////////////////////////////////////////
    //
    // Classes
    //
    ///////////////////////////////////////////////////////////////////////////////////////
     -->

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016295 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016295">
        <rdfs:label>neuronal ceroid lipofuscinosis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019262 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019262">
        <rdfs:label>juvenile neuronal ceroid lipofuscinosis</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016295"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020143"/>
        <oboInOwl:hasDbXref>icd11.foundation:1716107919</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>juvenile neuronal ceroid lipofuscinosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NANDO:2201243</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>JNCL</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Spielmeyer-Vogt disease</oboInOwl:hasExactSynonym>
        <ns4:IAO_0000115>A genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterized by onset at early school age with vision loss due to retinopathy, seizures and the decline of mental and motor capacities.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>batten disease</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0019262</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0004938</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:79264</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:1200154</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>juvenile NCL</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:0050756</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10052073</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:61663001</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/1716107919"/>
        <skos:closeMatch rdf:resource="http://identifiers.org/meddra/10052073"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/61663001"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020074"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020074 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020074">
        <rdfs:label>progressive myoclonus epilepsy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020143 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020143">
        <rdfs:label>cerebral lipidosis with dementia</rdfs:label>
    </Class>
</rdf:RDF>



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



