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    <!-- http://purl.obolibrary.org/obo/MONDO_0018866 -->

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        <rdfs:label>Aicardi-Goutieres syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0030362 -->

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        <rdfs:label>Aicardi-Goutieres syndrome 9</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/7365</ns3:IAO_0000233>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/aicardi_goutieres_syndrome_9</ns4:curated_content_resource>
        <oboInOwl:hasDbXref>UMLS:C5561966</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Aicardi-Goutieres syndrome 9</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>A type I interferonopathy characterized by severe developmental delay and progressive neurologic deterioration. Patients present in infancy with irritability and spasticity. Brain imaging shows diffusely abnormal white matter, cerebral atrophy, and intracranial calcification. Premature death has been associated with renal and/or hepatic failure.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>OMIM:619487</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0025553</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0030362</oboInOwl:id>
        <oboInOwl:hasDbXref>MEDGEN:1794176</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>AGS9</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0700263 -->

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        <rdfs:label>RNU7-1-related type 1 interferonopathy</rdfs:label>
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