Based on the candidate genes associated with HF development, we found that in the yellow, green, red, brown and turquoise modules (Fig. 6c), the core genes (LAMA5, ACVR1B, EGFR, FZD1, ITFB4, PTCH1, WNT5A, GLI2, LGR4, PTCH2, TGFβ2, LRP4, LRP5, FGF10, TGFβ3, BMPER, SOX10, WNT16, DKK1, TMEM79, BMP4, DSG4, ZDHHC21, SOSTDC1, TP63, RBPJ, FZD3, KRT25, WNT10A, WNT3, BMP7, KRT14, FZD4, and ITGA6) may be involved in the control of the HF development process. The gene discussed is WNT5A; the disease is hydrops fetalis.