2.16.840.1.113883.10.20.20.2/hgraph

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  1. Entry
     Clinical Genomic Statement (2.16.840.1.113883.10.20.20.2)
    1. Entry
       Indication Observation (2.16.840.1.113883.10.20.20.3.3)
    2. Entry
       Interpretive Phenotype (2.16.840.1.113883.10.20.20.2.5)
    3. Entry
       Genomic Source Class (2.16.840.1.113883.10.20.20.3.2)
    4. Entry
       Genomic Associated Observation (2.16.840.1.113883.10.20.20.4)
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