<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/DOID?iri=http://purl.obolibrary.org/obo/DOID_0060822"?>
<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:doid="http://purl.obolibrary.org/obo/doid#"
     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://www.geneontology.org/formats/oboInOwl#hasOBONamespace"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/doid#DO_rare_slim">
        <rdfs:label>DO_rare_slim</rdfs:label>
    </AnnotationProperty>
    <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.geneontology.org/formats/oboInOwl#inSubset"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    


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

    


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

    


    <!-- http://purl.obolibrary.org/obo/DOID_0060309 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_0060309">
        <rdfs:label xml:lang="en">syndromic X-linked intellectual disability</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/DOID_0060822 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_0060822">
        <rdfs:label xml:lang="en">syndromic X-linked intellectual disability Cabezas type</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_0060309"/>
        <oboInOwl:hasDbXref>ORDO:85293</oboInOwl:hasDbXref>
        <oboInOwl:id>DOID:0060822</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:13244</oboInOwl:hasDbXref>
        <oboInOwl:hasOBONamespace>disease_ontology</oboInOwl:hasOBONamespace>
        <ns3:IAO_0000115 xml:lang="en">A syndromic X-linked intellectual disability characterized by intellectual deficit, muscle wasting, short stature, hypogonadism, and abnormal gait, with variable occurrence of prominent lower lip, kyphosis, joint hyperextensibility, tremor, decreased fine motor coordination and impaired speech that has_material_basis_in mutation in the CUL4B gene on chromosome Xq24.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym xml:lang="en">Cabezas syndrome; syndromic X-linked mental retardation 15</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10CM:Q87.8</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MIM:300354</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym xml:lang="en">MRSS</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">MRXS15</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">MRXSC</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">X-linked mental retardation with short stature</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">X-linked mental retardation with short stature, hypogonadism, and abnormal gait</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">mental retardation, X-linked, syndromic 15</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">mental retardation, X-linked, syndromic 15 (Cabezas type)</oboInOwl:hasExactSynonym>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/doid#DO_rare_slim"/>
    </Class>
</rdf:RDF>



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



