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    <!-- http://purl.obolibrary.org/obo/MONDO_0009523 -->

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        <rdfs:label>Lichtenstein syndrome</rdfs:label>
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        <ns3:IAO_0000115>Lichstenstein syndrome is characterized by frequent infections associated with osteoporosis, a tendency for fractures and osseous anomalies. It has been described in two monozygotic twin brothers. Transmission is autosomal recessive.</ns3:IAO_0000115>
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        <oboInOwl:hasDbXref>SCTID:763668009</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>neutropenia immunoglobulin deficiency peculiar facies and bony anomalies</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:2390</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>GARD:0003248</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C535894</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:246550</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:340889</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Lichtenstein syndrome</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015134 -->

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        <rdfs:label>constitutional neutropenia</rdfs:label>
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