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Rhabdoid tumor of the kidney

MONDO:0002729

A rhabdoid tumor that arises from the kidney. It occurs in children and it is associated with abnormalities of chromosome 22. It is characterized by the presence of cells with a large eccentric nucleus, prominent nucleolus, and abundant cytoplasm. The prognosis is poor.

Also known as: MRTK, kidney rhabdoid tumor, kidney rhabdoid tumour, malignant rhabdoid tumor of kidney, malignant rhabdoid tumor of the kidney, malignant rhabdoid tumour of kidney, malignant rhabdoid tumour of the kidney, renal rhabdoid neoplasm

2859 clinical trials for this condition and its sub-types, 7 tagged with Rhabdoid tumor of the kidney itself.

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