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    <!-- http://purl.obolibrary.org/obo/MONDO_0012444 -->

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        <rdfs:label>neurodegeneration with brain iron accumulation 2B</rdfs:label>
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        <oboInOwl:hasExactSynonym>NBIA2B</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>neuroaxonal dystrophy, atypical</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>DOID:0110736</oboInOwl:hasDbXref>
        <rdfs:comment>NBIA2A is caused by homozygous or compound heterozygous mutation in the PLA2G6 gene; See also NBIA2B (610217), an overlapping disorder with later onset.</rdfs:comment>
        <oboInOwl:hasDbXref>NANDO:1200538</oboInOwl:hasDbXref>
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        <oboInOwl:hasRelatedSynonym>early-onset progressive cerebellar ataxia dystonia spasticity and intellectual decline</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasRelatedSynonym>atypical neuroaxonal dystrophy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>neurodegeneration with brain iron accumulation type 2B</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>NBIA2b</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:346658</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0010688</oboInOwl:hasDbXref>
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