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    <!-- http://purl.obolibrary.org/obo/MONDO_0005015 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005015">
        <rdfs:label>diabetes mellitus</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008812 -->

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        <rdfs:label>AREDYLD syndrome</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5723</ns4:IAO_0000233>
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        <oboInOwl:hasDbXref>MESH:C537427</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:1133</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>acrorenal defect-ectodermal dysplasia-diabetes syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>acrorenal Field defect, ectodermal dysplasia, and lipoatrophic diabetes</oboInOwl:hasRelatedSynonym>
        <ns4:IAO_0000115>AREDYLD stands for acral-renal-ectodermal-dysplasia-lipoatrophic-diabetes. This syndrome has been described in three individuals, one of whom was born to consanguineous parents. All patients had lipoatrophy, diabetes mellitus, generalized hypotrichosis, ectodermal dysplasia, renal alterations, dental abnormalities and other manifestations. It is probably transmitted as an autosomal recessive trait.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>MEDGEN:87435</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:237610008</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>acral renal ectodermal dysplasia lipoatrophic diabetes</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C0342280</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0008812</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0008509</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:753.3</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019287 -->

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        <rdfs:label>ectodermal dysplasia syndrome</rdfs:label>
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