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    <!-- http://purl.obolibrary.org/obo/MONDO_0017305 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017305">
        <rdfs:label>syndromic oculocutaneous albinism</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018306 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018306">
        <rdfs:label>Griscelli syndrome</rdfs:label>
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        <oboInOwl:hasExactSynonym>Griscelli-PruniC)ras syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIMPS:214450</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0018306</oboInOwl:id>
        <oboInOwl:hasDbXref>DOID:0060831</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0398794</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Griscelli disease</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NANDO:1200640</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Ch��diak-Higashi-like syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Griscelli-Pruni��ras syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:585090</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:37548006</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Griscelli syndrome (GS) is characterized by silvery gray sheen of the hair and hypopigmentation of the skin which can be associated to neurological impairment (type 1), immunodeficiency (type 2) or be isolated (type 3).</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>partial albinism-immunodeficiency syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:270.2</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0010913</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Griscelli-Pruniéras syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Chédiak-Higashi-like syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>ChC)diak-Higashi-like syndrome</oboInOwl:hasExactSynonym>
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    <!-- http://www.orpha.net/ORDO/Orphanet_381 -->

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        <rdfs:label>Griscelli disease</rdfs:label>
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