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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

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        <rdfs:label>hereditary disease</rdfs:label>
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    <!-- http://www.ebi.ac.uk/efo/EFO_0010644 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0010644">
        <rdfs:label xml:lang="en">Developmental delay with variable intellectual impairment and behavioural abnormalities</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0003847"/>
        <oboInOwl:hasExactSynonym>DDVIBA</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>Developmental delay with variable intellectual impairment and behavioral abnormalities (DDVIBA) is an autosomal dominant neurodevelopmental disorder. Most patients have impaired intellectual development with speech difficulties, and many have behavioral abnormalities, most commonly autism spectrum disorder (ASD), defects in attention, and/or hyperactivity. Many patients have dysmorphic features, although there is not a consistent gestalt. Additional more variable features may include hypotonia, somatic overgrowth with macrocephaly, mild distal skeletal anomalies, sleep disturbances, movement disorders, and gastrointestinal issues, such as constipation. The phenotype is highly variable (summary by Vetrini et al., 2019 and Torti et al., 2019).</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>OMIM:618430</oboInOwl:hasDbXref>
        <ns4:definition_citation>MedGen:CN258437</ns4:definition_citation>
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