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    <!-- http://purl.obolibrary.org/obo/NCIT_R176 -->

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    <!-- http://purl.obolibrary.org/obo/NCIT_C165258 -->

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        <rdfs:label>Cellosaurus Disease Terminology</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/NCIT_C175210 -->

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        <rdfs:label>Neurodegeneration with Brain Iron Accumulation 5</rdfs:label>
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        <ns4:NCIT_P207>C3550973</ns4:NCIT_P207>
        <ns4:IAO_0000115>An X-linked dominant condition caused by mutation(s) in the WDR45 gene, encoding WD repeat domain phosphoinositide-interacting protein 4. it is characterized by global developmental delay in early childhood, and subsequent dystonia and dementia in young adulthood.</ns4:IAO_0000115>
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