Subsequent studies have shown that the Lonp1 gene is associated with the occurrence and development of various diseases and conditions, including neurological disorders such as Parkinson’s disease [23], cardiovascular diseases [4, 24], neurodegenerative diseases [25], chronic kidney disease [26], skeletal muscle abnormalities [27], cancer, and mitochondrial diseases [10]. The gene discussed is LONP1; the disease is inborn mitochondrial metabolism disorder.