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        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/3776 -->

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        <rdfs:label>AFF2</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0010659 -->

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        <rdfs:label>FRAXE intellectual disability</rdfs:label>
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        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/2378/fragile-xe-syndrome</rdfs:seeAlso>
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        <oboInOwl:hasRelatedSynonym>mental retardation, X-linked, associated with fragile site FRAXE</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>fragile XE syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>FRAXE intellectual disability</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0751157</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>FRAXE syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:100973</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:155512</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>DOID:0080984</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:309548</oboInOwl:hasDbXref>
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        <ns5:IAO_0000115>A nonsyndromic X-linked mental retardation (NS-XLMR) characterized by mild intellectual deficit. FRAXE is the most common form of NS-XLMR.</ns5:IAO_0000115>
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        <oboInOwl:hasDbXref>SCTID:716709002</oboInOwl:hasDbXref>
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