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

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        <rdfs:label>syndromic oculocutaneous albinism</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018306 -->

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        <oboInOwl:hasDbXref>OMIMPS:214450</oboInOwl:hasDbXref>
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        <oboInOwl:hasRelatedSynonym>Griscelli disease</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NANDO:1200640</oboInOwl:hasDbXref>
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        <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>
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        <oboInOwl:hasDbXref>GARD:0010913</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Griscelli-Pruniéras syndrome</oboInOwl:hasExactSynonym>
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