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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_0005172 -->

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        <rdfs:label>skeletal system disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0012282 -->

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        <rdfs:label>Al-Gazali syndrome</rdfs:label>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6751</ns3:IAO_0000233>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/8522</ns3:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/10054/al-gazali-syndrome</rdfs:seeAlso>
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        <oboInOwl:hasRelatedSynonym>Al Gazali syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Al Gazali Al Talabani syndrome</oboInOwl:hasRelatedSynonym>
        <ns3:IAO_0000115>An autosomal recessive syndrome characterized by joint contractures, skeletal abnormalities, anterior segment anomalies of the eye and early lethality.</ns3:IAO_0000115>
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        <oboInOwl:hasDbXref>Orphanet:2725</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>MEDGEN:373020</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0010054</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C536817</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015327 -->

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