<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/MONDO?iri=http://purl.obolibrary.org/obo/MONDO_0002803"?>
<rdf:RDF xmlns="http://www.w3.org/2002/07/owl#"
     xml:base="http://www.w3.org/2002/07/owl"
     xmlns:mondo="http://purl.obolibrary.org/obo/mondo#"
     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: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#gard_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/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <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_0002803 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002803">
        <rdfs:label>intestinal pseudo-obstruction</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0004567"/>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/6789/intestinal-pseudo-obstruction</rdfs:seeAlso>
        <oboInOwl:hasExactSynonym>intestine pseudoobstruction</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0006789</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>pseudo-obstruction of intestine</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:569.89</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Intestinal pseudo-obstruction is a digestive disorder in whichthe intestinal walls are unable to contract normally (called hypomotility); the conditionresembles a true obstruction, but no actual blockage exists. Signs and symptoms may include abdominal pain; vomiting; diarrhea; constipation; malabsorption of nutrients leading to weight loss and/or failure to thrive ; and other symptoms. It may be classified as neuropathic (from lack of nerve function)or myopathic (from lack of muscle function), depending on the source of the abnormality. The condition is sometimes inherited (in an X-linked recessive or autosomal dominant manner)and may be caused by mutations in the FLNA gene; it may also be acquired after certain illnesses. The goal of treatment is to provide relief from symptoms andensure that nutritional support is adequate.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>MESH:D007418</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0002803</oboInOwl:id>
        <oboInOwl:hasDbXref>SCTID:235825006</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:3878</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C34733</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>hollow visceral myopathy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Chronic intestinal pseudo-obstruction.</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>intestinal pseudoobstruction</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>intestinal pseudo-obstruction</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0021847</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:5864</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/5864"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D007418"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/235825006"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0021847"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/NCIT_C34733"/>
        <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#rare"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0004567 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0004567">
        <rdfs:label>ileus</rdfs:label>
    </Class>
</rdf:RDF>



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



