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        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/25481 -->

    <Class rdf:about="http://identifiers.org/hgnc/25481">
        <rdfs:label>TRMU</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0000023 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000023">
        <rdfs:label>infantile liver failure</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0013111 -->

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        <rdfs:label>acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4521</ns4:IAO_0000233>
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        <rdfs:comment>Editor note: add transient course</rdfs:comment>
        <oboInOwl:hasExactSynonym>acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:480294</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>acute infantile liver failure due to synthesis defect of mitochondrial DNA-encoded proteins</oboInOwl:hasExactSynonym>
        <ns4:IAO_0000115>Acute infantile liver failure due to mtDNA-encoded proteins synthesis defect is a very rare mitochondrial respiratory chain deficiency described in fewer than 10 infants, primarily of middle Eastern descent, and characterized clinically by transient but life-threatening liver failure with elevated liver enzymes, jaundice, vomiting, coagulopathy, hyperbilirubinemia, and lactic acidemia.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>DOID:0080778</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016387 -->

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