CDC73 and Hyperparathyroidism-jaw tumor syndrome: Other genetic syndromes linked with ccRCC are hereditary paraganglioma–pheochromocytoma syndrome (PGL/PCC), which involves mutations in the succinate dehydrogenase (SDH) gene, hyperparathyroidism-jaw tumor syndrome (HPT-JT), characterized by mutations in cell division cycle (CDC73) gene and tuberous sclerosis complex (TSC) [46,47,48].