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    <!-- http://purl.obolibrary.org/obo/MONDO_0012824 -->

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        <rdfs:label>hypomyelinating leukodystrophy 4</rdfs:label>
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        <oboInOwl:hasExactSynonym>HLD4</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>MEDGEN:383026</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0060789</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Pelizaeus-Merzbacher-like disease due to HSPD1 mutation</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasExactSynonym>leukodystrophy, hypomyelinating, type 4</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>NANDO:1200581</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>hypomyelinating leukodystrophy type 4</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:612233</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0012824</oboInOwl:id>
        <oboInOwl:hasExactSynonym>mitochondrial HSP60 chaperonopathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0017294</oboInOwl:hasDbXref>
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        <rdfs:label>Pelizaeus-Merzbacher-like disease due to HSPD1 mutation</rdfs:label>
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