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    <!-- http://purl.obolibrary.org/obo/MONDO_0005328 -->

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        <rdfs:label>eye disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0010001 -->

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        <rdfs:label>ectodermal dysplasia-blindness syndrome</rdfs:label>
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        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/rodrigues_blindness</ns4:curated_content_resource>
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        <oboInOwl:hasDbXref>GARD:0002045</oboInOwl:hasDbXref>
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        <ns3:IAO_0000115>Ectodermal dysplasia-blindness syndrome is characterized by intellectual deficit, blindness caused by ocular malformations (microphthalmia, microcornea and sclerocornea), short stature, dysmorphic facial features (narrow nasal bridge and prominent ears), hypotrichosis, and malaligned teeth. It has been described in two siblings (brother and sister) and is likely to be transmitted as an autosomal recessive trait.</ns3:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>microphthalmos, microcornea, and sclerocornea with short stature and hair and dental abnormalities</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>OMIM:268320</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019287 -->

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        <rdfs:label>ectodermal dysplasia syndrome</rdfs:label>
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