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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_0010662 -->

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        <rdfs:label>paraplegia-intellectual disability-hyperkeratosis syndrome</rdfs:label>
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        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/paraplegia_intellectual_disability_hyperkeratosis_syndrome</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>MEDGEN:411554</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>mental retardation with spastic paraplegia and palmoplantar hyperkeratosis</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MESH:C537058</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0010662</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:2824</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:309560</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Fitzsimmons-McLachlan-Gilbert syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C2745996</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A syndrome characterized by intellectual deficit, spasticity in the lower limbs (spastic paraplegia), pes cavus deformity of both feet, an abnormal gait, and palmar and plantar hyperkeratosis. It has been reported in four brothers. The mother of the affected boys had normal intelligence, plantar hyperkeratosis and a strong facial resemblance to her retarded sons. Her three daughters were normal. This syndrome most likely an X-linked recessive condition.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:0002344</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015159 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020119 -->

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        <rdfs:label>X-linked syndromic intellectual disability</rdfs:label>
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