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    <!-- http://purl.obolibrary.org/obo/MONDO_0012350 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0012350">
        <rdfs:label>complement factor H deficiency</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016061 -->

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        <rdfs:label>immunodeficiency with factor H anomaly</rdfs:label>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9925</ns5:IAO_0000233>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/immunodeficiency_with_factor_h_anomaly</ns2:curated_content_resource>
        <oboInOwl:id>MONDO:0016061</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0017099</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:200421</oboInOwl:hasDbXref>
        <ns5:IAO_0006012>2026-04-01</ns5:IAO_0006012>
        <oboInOwl:hasDbXref>icd11.foundation:946399055</oboInOwl:hasDbXref>
        <rdfs:comment>This term is scheduled to be merged with MONDO:0012350 complement factor H deficiency, based on the fact that the concept of these 2 terms are the same. This ID will therefore be obsoleted and replaced with MONDO:0012350</rdfs:comment>
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