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    <!-- http://purl.obolibrary.org/obo/MONDO_0000508 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000508">
        <rdfs:label>syndromic intellectual disability</rdfs:label>
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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_0006025 -->

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        <rdfs:label>autosomal recessive disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019282 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019282">
        <rdfs:label>obsolete syndromic hair shaft abnormality</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0022316 -->

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        <rdfs:label>hair defect with photosensitivity and intellectual disability syndrome</rdfs:label>
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        <oboInOwl:hasRelatedSynonym>hair defect with photosensitivity and mental retardation</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Calderón-González-Cantu syndrome</oboInOwl:hasExactSynonym>
        <ns4:IAO_0000115>Syndrome with the association of stubby, coarse, sparse and fragile hair, eyebrows and eyelashes with photosensitivity and nonprogressive intellectual deficit, without a demonstrable metabolic aberration. It has been described in three sisters born to consanguineous parents.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>SCTID:721007005</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>kinky hair, photosensitivity, broken eyebrows and eyelashes, and nonprogressive mental retardation</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0022316</oboInOwl:id>
        <oboInOwl:hasExactSynonym>hair defect-photosensitivity-intellectual disability syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:234030</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Calderon Gonzalez-Cantu syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:383868</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>UMLS:C1856241</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C537628</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:1408</oboInOwl:hasDbXref>
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