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    <!-- http://purl.obolibrary.org/obo/DOID_891 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_891">
        <rdfs:label>progressive myoclonus epilepsy</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100036"/>
        <ns4:fromEPILONT rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</ns4:fromEPILONT>
        <ns4:fromILAE rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</ns4:fromILAE>
        <ns2:IAO_0000115>A variable age at onset electroclinical syndrome characterised by a relentlessly progressive disease course until death.</ns2:IAO_0000115>
        <oboInOwl:hasDbXref>OMIM:310370</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SNOMEDCT_US_2018_03_01:89480000</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>progressive Myoclonus epilepsy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:PS254800</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>progressive myoclonic epilepsy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDefinition>Progressive myoclonus epilepsy should considered in a patient with myoclonic seizures, with or without generalized tonic-clonic seizures in the following settings:
Progressive cognitive decline , Myoclonus resulting in progressive motor impairment, Cerebellar signs , Background slowing on EEG (particularly if increasing over time), Myoclonus that is refractory to trials of appropriate anti-seizure medication</oboInOwl:hasDefinition>
        <oboInOwl:hasDbXref>MESH:D020191</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>PME</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:7140</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCI2004_11_17:C7636</oboInOwl:hasDbXref>
        <rdfs:comment>OMIM mapping confirmed by DO. [SN].
OMIM mapping submitted by NeuroDevNet. [LS].</rdfs:comment>
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