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Hereditary papillary renal cell carcinoma

MONDO:0003789

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, hereditary papillary renal cell carcinoma, renal cell carcinoma, papillary

2770 clinical trials for this condition and its sub-types, 2 tagged with Hereditary papillary renal cell carcinoma itself.

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