This analysis revealed that subtype 1 was enriched in gene lists for immune signaling and Huntington’s and Parkinson’s disease, subtype 2 was enriched in gene lists for DNA repair and cell cycle signaling, subtype 3 was enriched in gene lists for classic oncogenes such as Notch and mTOR signaling, subtype 4 was enriched in gene lists for metabolism signaling, subtype 5 was enriched in gene sets for HIV/immune signaling, and subtype 6 was enriched in gene lists for apoptosis. Here, MTOR is linked to Parkinson disease.