We selected the LD-localized GO terms and identified seven DEGs; among them, lss was significantly downregulated, whereas retinol dehydrogenase 10b (rdh10b), dhrs3a, lysophosphatidylcholine acyltransferase 1 (lpcat1), abhydrolase domain containing 4 (abhd4), dhrs3b, and LD-associated hydrolase (ldah) were significantly upregulated in cells in HFM (Figure 1D). The gene discussed is LPCAT1; the disease is craniofacial microsomia.