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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_1547">
        <rdfs:label>Cryptomicrotia - brachydactyly - excess fingertip arch</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_183530"/>
        <oboInOwl:hasDbXref>ICD10:Q87.8</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Tonoki-Ohura-Niikawa syndrome</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>Cryptomicrotia - brachydactyly - excess fingertip arch syndrome describes a combination of malformations that include bilateral cryptomicrotia, brachytelomesophalangy with short middle and distal phalanges of digits 2 through 5, hypoplastic toenails and excess fingertip arch patterns, and has been reported in one family (mother and son). Cryptomicrotia - brachydactyly - excess fingertip arch syndrome is thought to follow an autosomal dominant transmission. There have been no further descriptions in the literature since 1988.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>OMIM:123560</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Cryptomicrotia-brachydactyly syndrome</oboInOwl:hasExactSynonym>
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        <rdfs:label>Rare genetic developmental defect during embryogenesis</rdfs:label>
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