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    <!-- http://purl.obolibrary.org/obo/MONDO_0005093 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005093">
        <rdfs:label>skin disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0007526 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007526">
        <rdfs:label>Ehlers-Danlos syndrome, spondylodysplastic type</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015327"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019052"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020066"/>
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        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/ehlers_danlos_syndrome_spondylodysplastic_type_1</ns2:curated_content_resource>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/ehlers_danlos_syndrome_spondylodysplastic_type_2</ns2:curated_content_resource>
        <oboInOwl:hasRelatedSynonym>Ehlers-Danlos syndrome, progeroid type (former)</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasNarrowSynonym>dermatan sulphate proteoglycan</oboInOwl:hasNarrowSynonym>
        <ns4:IAO_0000115>A form of Ehlers-Danlos syndrome characterized by a premature aging with sparse hair, macrocephaly, loose elastic skin, failure to thrive, joint laxity, psychomotor retardation, hypotonia, and defective wound healing with atrophic scars.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>galactosyltransferase I deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C536201</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:720861000</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>PDS</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>EDS, progeroid type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasNarrowSynonym>Ehlers-Danlos syndrome, spondylodysplastic type, 1</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasExactSynonym>B4GALT7-CDG</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>defective biosynthesis of proteodermatan sulphate</oboInOwl:hasExactSynonym>
        <oboInOwl:hasNarrowSynonym>proteodermatan sulfate, defective biosynthesis of</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasDbXref>GARD:0009991</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>spondylodysplastic Ehlers-Danlos syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasNarrowSynonym>Ehlers-Danlos syndrome with short stature and limb anomalies</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>Pds, defective biosynthesis of</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>EDSSPD1</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>dermatan sulfate proteoglycan</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>xylosylprotein 4-beta-galactosyltransferase deficiency</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasNarrowSynonym>XGPT deficiency</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasDbXref>DOID:0050802</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:75496</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007526</oboInOwl:id>
        <oboInOwl:hasExactSynonym>defective biosynthesis of proteodermatan sulfate</oboInOwl:hasExactSynonym>
        <oboInOwl:hasNarrowSynonym>galactosyltransferase 1 deficiency</oboInOwl:hasNarrowSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015327 -->

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        <rdfs:label>developmental anomaly of metabolic origin</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019052 -->

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        <rdfs:label>inborn errors of metabolism</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020066 -->

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        <rdfs:label>Ehlers-Danlos syndrome</rdfs:label>
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        <rdfs:label>Ehlers-Danlos syndrome, progeroid type</rdfs:label>
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