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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0007639 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007639">
        <rdfs:label>fundus albipunctatus</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0016420"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100443"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100444"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_1040055"/>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/fundus_albipunctatus</ns4:curated_content_resource>
        <oboInOwl:hasBroadSynonym>retinitis punctata albescens</oboInOwl:hasBroadSynonym>
        <oboInOwl:hasDbXref>DOID:11105</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0311338</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:362.74</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:1981512475</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:362.76</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>fundus albipunctatus</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:68222009</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:136880</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:227796</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007639</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0013809</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>pigmentary retinal dystrophy</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>Fundus albipunctatus is a rare, genetic retinal dystrophy characterized by the presence of numerous small, round, yellowish-white retinal lesions that are distributed throughout the retina but spare the fovea. Patients present in childhood with non-progressive night blindness with prolonged cone and rod adaptation times. The macula may or may not be involved, which may result in a decrease of central visual acuity with age.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>MESH:C562733</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:86317</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016420 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016420">
        <rdfs:label>familial flecked retinopathy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100443 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100443">
        <rdfs:label>RDH5-related retinopathy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0100444 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100444">
        <rdfs:label>RLBP1-related retinopathy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_1040055 -->

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        <rdfs:label>PRPH2-related retinopathy</rdfs:label>
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