Other syndromes include BAP1 mutant disease, hereditary leiomyomatosis and RCC, Birt–Hogg–Dube syndrome, familial ccRCC with chromosome 3 translocation, phosphatase and tension homolog hamartoma syndrome, hereditary pRCC, succinate dehydrogenase (SDH) deficient RCC, and tuberous sclerosis complex. The gene discussed is BAP1; the disease is renal cell carcinoma.