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    <!-- http://www.orpha.net/ORDO/Orphanet_355 -->

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        <rdfs:label>obsolete_Gaucher disease</rdfs:label>
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        <ns5:reason_for_obsolescence>Replaced with Mondo term.</ns5:reason_for_obsolescence>
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        <oboInOwl:hasDbXref>ICD10:E75.2</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Gaucher disease (GD) is a lysosomal storage disorder encompassing three main forms (types 1, 2 and 3), a fetal form and a variant with cardiac involvement (Gaucher disease - ophthalmoplegia - cardiovascular calcification or Gaucher-like disease) (see these terms).</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>OMIM:230900</oboInOwl:hasDbXref>
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