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    <!-- http://purl.obolibrary.org/obo/DOID_0050325 -->

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        <rdfs:label>genetic disorder</rdfs:label>
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        <rdfs:label>hereditary multiple exostoses</rdfs:label>
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        <ns2:IAO_0000118>&quot;Multiple exostosis syndromes&quot; EXACT [SNOMEDCT_2005_07_31:240186007]</ns2:IAO_0000118>
        <rdfs:seeAlso>SNOMEDCT_2010_1_31:84852005</rdfs:seeAlso>
        <rdfs:seeAlso>OMIM2009_05_01:133700</rdfs:seeAlso>
        <rdfs:seeAlso>SNOMEDCT_2010_1_31:254044004</rdfs:seeAlso>
        <rdfs:seeAlso>SNOMEDCT_2010_1_31:205479007</rdfs:seeAlso>
        <rdfs:seeAlso>SNOMEDCT_2010_1_31:16535008</rdfs:seeAlso>
        <ns2:IAO_0000118>&quot;multiple exostosis&quot; EXACT [CSP2005:1849-1975]</ns2:IAO_0000118>
        <rdfs:seeAlso>MSH2010_2010_02_22:D005097</rdfs:seeAlso>
        <rdfs:seeAlso>SNOMEDCT_2010_1_31:240186007</rdfs:seeAlso>
        <rdfs:seeAlso>UMLS_CUI:C0015306</rdfs:seeAlso>
        <rdfs:seeAlso>URI: http://www.ebi.ac.uk/cellline#hereditary_multiple_exostoses</rdfs:seeAlso>
        <rdfs:seeAlso>NCI2009_04D:C5183</rdfs:seeAlso>
        <ns2:IAO_0000118>&quot;Osteochondromatosis syndrome (disorder) [Ambiguous]&quot; EXACT [SNOMEDCT_2005_07_31:16535008]</ns2:IAO_0000118>
        <ns2:IAO_0000118>&quot;Multiple exostoses type I&quot; EXACT [SNOMEDCT_2005_07_31:254044004]</ns2:IAO_0000118>
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