<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0018953"?>
<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:ns4="http://purl.obolibrary.org/obo/mondo#"
     xmlns:foaf="http://xmlns.com/foaf/0.1/"
     xmlns:dc="http://purl.org/dc/elements/1.1/"
     xmlns:ns3="http://purl.obolibrary.org/obo/">
    


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

    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#otar"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.w3.org/2004/02/skos/core#exactMatch"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#clingen"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#inSubset"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#should_conform_to"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/MONDO_0018075 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018075">
        <rdfs:label>neural tube defect</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0018230 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018230">
        <rdfs:label>skeletal dysplasia</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0018953 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018953">
        <rdfs:label>parietal foramina</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0018075"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0018230"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100545"/>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/parietal_foramina</ns4:curated_content_resource>
        <oboInOwl:hasExactSynonym>symmetric parietal foramina</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>enlarged parietal foramina</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:905361904</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:168500</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>parietal foramina</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>hereditary cranium bifidum</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0016662</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:60015</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>fenestrae parietales symmetricae</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:0060285</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0018953</oboInOwl:id>
        <oboInOwl:hasDbXref>SCTID:718099006</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>HP:0002697</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C566826</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>foramina parietalia permagna</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>Enlarged parietal foramina (EPF) is a developmental defect, characterized by variable intramembranous ossification defects of the parietal bones, which is either asymptomatic, symptomatic (headaches, nausea, vomiting, intellectual disability) or associated with other pathologies.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>catlin marks</oboInOwl:hasExactSynonym>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/905361904"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C566826"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/718099006"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0060285"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#clingen"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
        <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#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#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <ns4:should_conform_to rdf:resource="http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_60015"/>
        <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS168500"/>
        <ns4:curated_content_resource rdf:resource="https://search.clinicalgenome.org/kb/conditions/MONDO:0018953"/>
    </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 -->



