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        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/16412 -->

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    <!-- http://purl.obolibrary.org/obo/MONDO_0014472 -->

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        <rdfs:label>periodic fever-infantile enterocolitis-autoinflammatory syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>MEDGEN:863504</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0017725</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>AUTOINFLAMMATION with infantile enterocolitis</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>NLRC4-related MAS</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>NORD:1939</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0014472</oboInOwl:id>
        <oboInOwl:hasExactSynonym>NLRC4-related macrophage activation syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>NLRC4-related autoinflammatory syndrome with macrophage activation syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Autoinflammation with Infantile Enterocolitis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>autoinflammation with infantile enterocolitis</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>NANDO:2200459</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:436166</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:616050</oboInOwl:hasDbXref>
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        <rdfs:label>hereditary periodic fever syndrome</rdfs:label>
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