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    <!-- http://purl.obolibrary.org/obo/MONDO_0007215 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007215">
        <rdfs:label>brachydactyly type A1</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0021004"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0975810"/>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4948</ns3:IAO_0000233>
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        <oboInOwl:hasExactSynonym>brachydactyly, Farabee type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:354673</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>Orphanet:93388</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>DOID:0110964</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:112500</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A rare, congenital limb malformation characterized by shortened or underdeveloped middle phalanges of all digits, that are sometimes fused with the terminal phalanges. The proximal phalanges of the thumbs and big toes are also shortened. Short stature in adulthood has been reported in association.</ns3:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021004 -->

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        <rdfs:label>brachydactyly</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0975810 -->

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        <rdfs:label>short stature with nonspecific skeletal abnormalities</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_93388 -->

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        <rdfs:label>obsolete_brachydactyly type A1</rdfs:label>
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