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    <!-- http://purl.obolibrary.org/obo/MONDO_0010908 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010908">
        <rdfs:label>loose anagen syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0011899 -->

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        <rdfs:label>Noonan syndrome-like disorder with loose anagen hair</rdfs:label>
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        <oboInOwl:hasDbXref>MEDGEN:334697</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>NSLH</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>UMLS:C1843181</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:607721</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C564342</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C178129</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Tosti syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:2701</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0080691</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>NSLH1</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>NS/LAH</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0010719</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:723444009</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Noonan-like syndrome with loose anagen hair (NS/LAH) is a Noonan-related syndrome, characterized by facial anomalies suggestive of Noonan syndrome ; a distinctive hair anomaly described as loose anagen hair syndrome ; frequent congenital heart defects; distinctive skin features with darkly pigmented skin, keratosis pilaris, eczema or occasional neonatal ichtyosis ; and short stature, often associated with a GH deficiency and psychomotor delays.</ns3:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015160 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020297 -->

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