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    <!-- http://purl.obolibrary.org/obo/MONDO_0000470 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000470">
        <rdfs:label>endocardium disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0009169 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0009169">
        <rdfs:label>endocardial fibroelastosis</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000470"/>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/6336/endocardial-fibroelastosis</rdfs:seeAlso>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/endocardial_fibroelastosis</ns2:curated_content_resource>
        <oboInOwl:hasRelatedSynonym>EFE</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:1971033419</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0014117</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2022</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10CM:I42.4</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>EFO:0007251</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:4041</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Elastomyofibrosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NORD:1090</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>endocardial fibroelastosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:65457005</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D004695</oboInOwl:hasDbXref>
        <rdfs:comment>Editor notes: ORDO classifies as both familial and non-familial</rdfs:comment>
        <oboInOwl:hasDbXref>NCIT:C98922</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:425.3</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Endomyocardial fibroelastosis is a cause of unexplained childhood cardiac insufficiency. It results from diffuse thickening of the endocardium leading to dilated myocardiopathy in the majority of cases and restrictive myocardiopathy in rare cases. It may occur as a primary disorder or may be secondary to another cardiac malformation, notably aortic stenosis or atresia.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>NANDO:2100060</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0006336</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2200235</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0009169</oboInOwl:id>
        <oboInOwl:hasDbXref>MedDRA:10014663</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:226000</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:12929</oboInOwl:hasDbXref>
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        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016340"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016333 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016333">
        <rdfs:label>familial dilated cardiomyopathy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016338 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016338">
        <rdfs:label>non-familial dilated cardiomyopathy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016340 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016340">
        <rdfs:label>familial restrictive cardiomyopathy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016345 -->

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        <rdfs:label>non-familial restrictive cardiomyopathy</rdfs:label>
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