hereditary papillary renal cell carcinoma (Monarch Disease Ontology entry MONDO_0003789) is a familial carcinoma inherited in an autosomal dominant trait. It is characterized by the development of multiple, bilateral papillary renal cell carcinomas. The carcinomas range from microscopic lesions to clinically symptomatic tumors. It is associated with activating mutations of the MET oncogene. Also known as: familial renal papillary carcinoma, hereditary kidney papillary carcinoma, hereditary papillary carcinoma of kidney, hereditary papillary carcinoma of the kidney, hereditary papillary renal carcinoma, hereditary papillary renal cell cancer, renal cell carcinoma, papillary, renal cell carcinoma, papillary, 1, familial and somatic.