<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/HTN?iri=http://purl.obolibrary.org/obo/DOID_0050177"?>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000412"/>
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    <!-- http://purl.obolibrary.org/obo/DOID_0050177 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_0050177">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">monogenic disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_630"/>
        <ns2:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">A genetic disease that is the result of one or more abnormal alleles and may be dominant (a single copy of the abnormal allele is sufficient to give rise to the disease), semi-dominant, or recessive (requiring both copies of the gene to have an abnormal allele).</ns2:IAO_0000115>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



