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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

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        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

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    <!-- http://purl.obolibrary.org/obo/MONDO_0016432 -->

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        <rdfs:label>heart-hand syndrome</rdfs:label>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6877</ns3:IAO_0000233>
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        <oboInOwl:hasExactSynonym>atriodigital dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0020573</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:1853290</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:228184</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Heart-hand syndrome refers to a group of congenital disorders characterized by malformations of the upper limbs and heart. To date, heart-hand syndrome comprises the following rare syndromes; Holt-Oram syndrome; heart-hand syndrome type 2; heart-hand syndrome type 3; heart hand syndrome, Slovenian type, brachydactyly-long thumb; and patent ductus arteriosus-bicuspid aortic valve - hand anomalies.</ns3:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018234 -->

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    <!-- http://purl.obolibrary.org/obo/MONDO_0019054 -->

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