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    <!-- http://purl.obolibrary.org/obo/RO_0004030 -->

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        <rdfs:label>disease arises from structure</rdfs:label>
        <rdfs:label>disease arises from alteration in structure</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/CHR_9606-chr3q26 -->

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        <rdfs:label>3q26 (Human)</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000762 -->

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        <rdfs:label>syndrome caused by partial chromosomal duplication</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016954 -->

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        <rdfs:label>partial duplication of the long arm of chromosome 3</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019878 -->

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        <rdfs:label>3q26 microduplication syndrome</rdfs:label>
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        <ns6:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/3492</ns6:IAO_0000233>
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        <oboInOwl:hasDbXref>UMLS:C4755319</oboInOwl:hasDbXref>
        <ns6:IAO_0000115>3q26 microduplication syndrome is a rare chromosomal anomaly characterized by prenatal and postnatal growth retardation, developmental delay, intellectual impairment, dysmorphic signs and variable combination of congenital anomalies, including cardiovascular, genitourinary and skeletal anomalies and spectrum of caudal malformations.</ns6:IAO_0000115>
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        <oboInOwl:hasDbXref>Orphanet:96095</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>dup(3)(q26)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Cornelia de Lange-like syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>trisomy 3q26</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020226 -->

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