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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_0009067 -->

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        <oboInOwl:hasDbXref>GARD:0006237</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>cystinuria-lysinuria syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasExactSynonym>cystinuria</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>DOID:9266</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Cystinuria is a renal tubular amino acid transport disorder characterized by recurrent formation of kidneys cystine stones.</ns3:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>cystinuria, type II, formerly</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>cystinuria-lysinuria</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>cystinuria, type A/B</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>Orphanet:214</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10CM:E72.01</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0010691</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C84664</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>cystinuria, type II</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>HP:0003131</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>CSNU</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasRelatedSynonym>cystinuria, type I</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MedDRA:10011778</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>NANDO:2200489</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:8226</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:85020001</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>cystinuria, type III, formerly</oboInOwl:hasRelatedSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015962 -->

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        <rdfs:label>inherited renal tubular disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019216 -->

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        <rdfs:label>inborn disorder of amino acid transport</rdfs:label>
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