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    <!-- http://purl.obolibrary.org/obo/MONDO_0000429 -->

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        <rdfs:label>autosomal genetic 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_0008428 -->

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        <rdfs:label>septooptic dysplasia</rdfs:label>
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        <oboInOwl:hasDbXref>MedDRA:10067159</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>septooptic dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:0060857</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Septooptic dysplasia (SOD) is a clinically heterogeneous disorder characterized by the classical triad of optic nerve hypoplasia, pituitary hormone abnormalities and midline brain defects.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>UMLS:C0338503</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>septo-optic dysplasia with growth hormone deficiency</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>hypopituitarism and septooptic &#39;dysplasia&#39;</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>SOD</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:182230</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>septo-optic dysplasia sequence</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0007627</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C85063</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:1200560</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:1200561</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>MESH:D025962</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:90926</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:3157</oboInOwl:hasDbXref>
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        <rdfs:label>Septo-optic dysplasia</rdfs:label>
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