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    <!-- http://purl.obolibrary.org/obo/MONDO_0005620 -->

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        <rdfs:label>cerebral amyloid angiopathy</rdfs:label>
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        <oboInOwl:hasDbXref>SCTID:230724001</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:85458</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10CM:I68.0</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>hereditary cerebral hemorrhage with amyloidosis - Dutch type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C1510489</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>HCHWA</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasRelatedSynonym>cerebral amyloid angiopathy, genetic</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>hereditary cerebral haemorrhage with amyloidosis - Dutch type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C84625</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Hereditary cerebral hemorrhage with amyloidosis (HCHWA) describes a group of rare familial central nervous system disorders characterized by amyloid deposition in the cerebral blood vessels leading to hemorrhagic and non-hemorrhagic strokes, focal neurological deficits, and progressive cognitive decline eventually leading to dementia.</ns3:IAO_0000115>
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        <oboInOwl:hasExactSynonym>dutch hereditary cerebral amyloid angiopathy</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>MEDGEN:267610</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:277.39</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0011057 -->

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        <rdfs:label>cerebrovascular disorder</rdfs:label>
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