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    <!-- http://purl.obolibrary.org/obo/MONDO_0008855 -->

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        <rdfs:label>MHC class II deficiency</rdfs:label>
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        <oboInOwl:hasDbXref>DOID:5812</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>BLS type II</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NCIT:C176823</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>BLS, type II</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>BARE lymphocyte syndrome, type II, complementation group C, included</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:2021339495</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2200702</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>BARE lymphocyte syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>immunodeficiency by defective expression of HLA class type 2</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:572</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>BARE lymphocyte syndrome, type II, complementation group B, included</oboInOwl:hasRelatedSynonym>
        <ns3:IAO_0000115>Immunodeficiency by defective expression of HLA class 2 is a rare primary genetic immunodeficiency disorder characterized by partial or complete absence of human leukocyte antigen class 2 expression resulting in severe defect in both cellular and humoral immune response to antigens. The disorder presents clinically as marked susceptibility to infections, severe malabsorption and failure to thrive and is often fatal in early childhood.</ns3:IAO_0000115>
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        <oboInOwl:hasDbXref>NANDO:1200329</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>severe combined immunodeficiency, HLA class ii-negative</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:1781237</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>major histocompatibility complex class II expression deficiency</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasRelatedSynonym>BLS 2</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>HLA class 2-negative SCID</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>NCIT:C3895</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>OMIMPS:209920</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>BLSII</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Bare lymphocyte syndrome, type II</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>BARE lymphocyte syndrome, type II, complementation group D, included</oboInOwl:hasRelatedSynonym>
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