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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0000486 -->

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        <rdfs:label>Strabismus</rdfs:label>
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        <rdfs:label>White eyebrow</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0002227 -->

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        <rdfs:label>White eyelashes</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000426 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000426">
        <rdfs:label>autosomal dominant disease</rdfs:label>
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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_0015161 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome without intellectual disability</rdfs:label>
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        <rdfs:label>obsolete neuro-ophthalmological disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018094 -->

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        <rdfs:label>Waardenburg syndrome</rdfs:label>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5682</ns5:IAO_0000233>
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        <oboInOwl:hasDbXref>OMIMPS:193500</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:9258</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Waardenburg syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C3266898</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0018094</oboInOwl:id>
        <oboInOwl:hasDbXref>MedDRA:10069203</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Van der Hoeve Halbertsma Waardenburg Gualdi syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Mende syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:473809</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0005525</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C85222</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1832</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>A disorder characterized by varying degrees of deafness and minor defects in structures arising from neural crest, including pigmentation anomalies of eyes, hair, and skin. WS is classified into four clinical and genetic phenotypes.</ns5:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019290 -->

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        <rdfs:label>hypopigmentation of the skin</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020191 -->

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        <rdfs:label>obsolete eyebrow/eyelashes pigmentation anomaly</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020276 -->

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        <rdfs:label>obsolete pigmentation disorder with eye involvement, excluding albinism</rdfs:label>
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