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    <!-- http://purl.obolibrary.org/obo/HP_0002143 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0002143">
        <rdfs:label>Abnormal spinal cord morphology</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_6001442 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_6001442">
        <rdfs:label>Spinal cord H sign</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0002143"/>
        <dcterms:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2025-12-17T15:52:15Z</dcterms:date>
        <ns4:IAO_0000115>The H sign can be ascertained by spinal magnetic resonance imaging (MRI) and represents spinal cord myelitis isolated to the gray matter. A longitudinally extensive T2 hyperintense spinal cord lesion from C6 to T10, predominantly involving the gray matter. The appearance of the anomaly is said to resemble the letter H.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>H sign in the spinal cord</oboInOwl:hasExactSynonym>
        <rdfs:comment>The H sign can be observed with Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD), multiple sclerosis, and other neuroimmunological diseases.</rdfs:comment>
        <ns4:IAO_0000233 rdf:resource="https://github.com/obophenotype/human-phenotype-ontology/issues/11361"/>
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