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    <!-- http://purl.obolibrary.org/obo/MONDO_0011476 -->

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        <rdfs:label>MHC class I deficiency</rdfs:label>
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        <oboInOwl:hasExactSynonym>Bare lymphocyte syndrome type 1</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>GARD:0009548</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:604571</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>NANDO:1200328</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0060009</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0011476</oboInOwl:id>
        <oboInOwl:hasDbXref>MEDGEN:346868</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>BLS type 1</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NANDO:2200701</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Immunodeficiency by defective expression of HLA class 1 is a very rare, primary, genetic, immunodeficiency disorder characterized by partial or complete absence of human leukocyte antigen class I expression resulting in a non-specific clinical picture of impaired immune response and susceptibility to infections.</ns4:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015131 -->

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        <rdfs:label>combined immunodeficiency</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015974 -->

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