Conversely, several pathways related to angiogenesis (Semaphorin Neuronal Repulsive Signaling Pathway, Ephrin Receptor Signaling, and Regulation of Insulin-like Growth Factor (IGF) Transport and Uptake by IGFBPs) and fibrosis (including Calcium Signaling; Dilated Cardiomyopathy Signaling Pathway; Hepatic Fibrosis Signaling Pathway; Dopamine-DARPP32 Feedback in cAMP Signaling; Smooth Muscle Contraction; Nuclear Cytoskeleton Signaling Pathway; and Formation of Fibrin Clot) were found to be deregulated in both groups. The gene discussed is PPP1R1B; the disease is dilated cardiomyopathy.