<?xml version="1.0"?>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasExactSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- 
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021147 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0021147">
        <rdfs:label>disorder of development or morphogenesis</rdfs:label>
    </Class>
    


    <!-- http://www.ebi.ac.uk/efo/EFO_0700056 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0700056">
        <rdfs:label>progressive cerebello-cerebral atrophy</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0021147"/>
        <ns3:IAO_0000115>A rare genetic neurological disorder characterized by postnatal onset of severe global developmental delay, profound mental retardation, progressive microcephaly, progressive spasticity evolving into spastic quadriplegia with joint contractures, generalized seizures, and irritability. Severe choreoathetosis and dysmorphic features are absent. Brain imaging shows progressive cerebellar atrophy followed by cerebral atrophy affecting both white and grey matter, but no pontine involvement.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>PCCA</oboInOwl:hasExactSynonym>
        <rdfs:comment>Term added in response to Mondo restructuring. To be considered for replacement or obsoletion in EFO also.</rdfs:comment>
        <oboInOwl:hasDbXref>Orphanet:247198</oboInOwl:hasDbXref>
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