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    <!-- http://purl.obolibrary.org/obo/MONDO_0000200 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000200">
        <rdfs:label>Zimmermann-Laband syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>GARD:0000385</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0796013</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C536725</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:135500</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A rare disorder characterized by gingival fibromatosis, coarse facial appearance, and absence or hypoplasia of nails or terminal phalanges of hands and feet.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>Laband syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Laband-Zimmermann syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>gingival fibromatosis, abnormal fingers, fingernails, nose and ears, and splenomegaly</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:208656</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>fibromatosis gingival, hepatosplenomegaly other anomalies</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Zimmerman Laband syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:759.89</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:699447001</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:8285962</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>ZLS1</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Zimmermann-Laband syndrome 1</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:3473</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Zimmermann-Laband syndrome type 1</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000508 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000508">
        <rdfs:label>syndromic intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

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        <rdfs:label>hereditary disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015159 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-intellectual disability</rdfs:label>
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