<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/EFO?iri=http://purl.obolibrary.org/obo/MONDO_0011475"?>
<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:ORDO="http://www.orpha.net/ORDO/"
     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://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <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#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_0011475 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0011475">
        <rdfs:label>Charcot-Marie-Tooth disease type 4B2</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0018995"/>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/9200/charcot-marie-tooth-disease-type-4b2</rdfs:seeAlso>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/charcot_marie_tooth_disease_demyelinating_type_4b2</ns4:curated_content_resource>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/charcot_marie_tooth_disease_type_4b2</ns4:curated_content_resource>
        <oboInOwl:hasExactSynonym>SBF2 Charcot-Marie-Tooth disease type 4</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C535421</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>CMT4B2</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Charcot-Marie-Tooth disease type 4B2</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:99956</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1858278</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Charcot Marie Tooth disease type 4B2</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Charcot-Marie-Tooth disease, type 4B2</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>CMT 4B2</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>DOID:0110190</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Charcot-Marie-Tooth disease type 4B2 (CMT4B2) is a subtype of Charcot-Marie-Tooth type 4 characterized by a severe, early childhood-onset of demyelinating sensorimotor neuropathy, early-onset glaucoma, focally folded myelin sheaths in the peripheral nerves, severely reduced nerve conduction velocities, and the typical CMT phenotype (i.e. distal muscle weakness and atrophy, sensory loss, and frequent pes cavus). Severe visual impairment leading to visual loss has also been reported.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>icd11.foundation:393759720</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0009200</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Charcot-Marie-Tooth disease type 4 caused by mutation in SBF2</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:715800000</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:604563</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0011475</oboInOwl:id>
        <oboInOwl:hasDbXref>MEDGEN:346869</oboInOwl:hasDbXref>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/393759720"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/medgen/346869"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C535421"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/715800000"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C1858278"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0110190"/>
        <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#orphanet_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_99956"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/604563"/>
        <ns4:curated_content_resource rdf:resource="https://search.clinicalgenome.org/kb/conditions/MONDO:0011475"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0018995 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018995">
        <rdfs:label>Charcot-Marie-Tooth disease type 4</rdfs:label>
    </Class>
    


    <!-- http://www.orpha.net/ORDO/Orphanet_99956 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_99956">
        <rdfs:label>obsolete_Charcot-Marie-Tooth disease type 4B2</rdfs:label>
    </Class>
</rdf:RDF>



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



