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    <!-- http://purl.obolibrary.org/obo/DOID_0050460 -->

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        <rdfs:label xml:lang="en">Wolf-Hirschhorn syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>MIM:194190</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>ICD10CM:Q93.3</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ORDO:280</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D054877</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>NCI:C35528</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>SNOMEDCT_US_2025_09_01:17122004</oboInOwl:hasDbXref>
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        <rdfs:comment xml:lang="en">OMIM mapping confirmed by DO. [LS].</rdfs:comment>
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        <ns3:IAO_0000115 xml:lang="en">A chromosomal deletion syndrome that is characterized by distinct craniofacial features, hypotonia and intellectual disability and has_material_basis_in a hemizygous deletion of chromosome 4p16.3.</ns3:IAO_0000115>
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