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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002254">
        <rdfs:label>syndromic disease</rdfs:label>
    </Class>
    


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

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


    <!-- http://purl.obolibrary.org/obo/MONDO_0010638 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010638">
        <rdfs:label>keratosis follicularis-dwarfism-cerebral atrophy syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/3099/keratosis-follicularis-dwarfism-and-cerebral-atrophy</rdfs:seeAlso>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/keratosis_follicularis_dwarfism_and_cerebral_atrophy_2</ns2:curated_content_resource>
        <oboInOwl:id>MONDO:0010638</oboInOwl:id>
        <oboInOwl:hasDbXref>MEDGEN:374340</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0003099</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2339</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>dwarfism, cerebral atrophy and generalised keratosis follicularis</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MESH:C536158</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>dwarfism, cerebral atrophy and generalized keratosis follicularis</oboInOwl:hasRelatedSynonym>
        <ns4:IAO_0000115>A syndrome characterized by generalized keratosis follicularis, severe proportionate dwarfism and cerebral atrophy. It has been described in six males from one family (three boys and three maternal uncles). Generalized alopecia and microcephaly were also present.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>OMIM:308830</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>keratosis follicularis dwarfism and cerebral atrophy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>keratosis follicularis, dwarfism, and cerebral atrophy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C1839910</oboInOwl:hasDbXref>
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        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/C536158"/>
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        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005093"/>
        <ns2:excluded_subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019268"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019268 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019268">
        <rdfs:label>epidermal disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020119 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020119">
        <rdfs:label>X-linked syndromic intellectual disability</rdfs:label>
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