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    <!-- http://purl.obolibrary.org/obo/MONDO_0011323 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0011323">
        <rdfs:label>arhinia, choanal atresia, and microphthalmia</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015161"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015770"/>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9882</ns3:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/8755/arhinia-choanal-atresia-microphthalmia</rdfs:seeAlso>
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        <oboInOwl:hasExactSynonym>Bosma arhinia-microphthalmia syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Bosma-Henkin-Christiansen syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:603457</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Bosma Henkin Christiansen syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>BAM syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>arhinia choanal atresia microphthalmia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C537429</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>BAMS</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Gifford-Bosma syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:2250</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0011323</oboInOwl:id>
        <oboInOwl:hasExactSynonym>arhinia, choanal atresia, microphthalmia, and hypogonadotropic hypogonadism</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Bosma arhinia microphthalmia syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Ruprecht Majewski syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:355084</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Any syndromic disease characterized by severe hypoplasia of the nose and eyes, palatal abnormalities, deficient taste and smell, inguinal hernias, hypogonadotropic hypogonadism with cryptorchidism, and normal intelligence that occurs due to variation in the SMCHD1 gene.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:0027263</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1863878</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:720511000</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Bosma syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Bosma Arhinia Microphthalmia Syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>arrhinia-choanal atresia-microphthalmia syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:1135</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015161 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome without intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015770 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015770">
        <rdfs:label>congenital hypogonadotropic hypogonadism</rdfs:label>
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        <rdfs:label>Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism</rdfs:label>
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