Rhabdoid tumor (RT) is an aggressive pediatric soft tissue sarcoma that arises in the kidney, the liver, the peripheral nerves and all miscellaneous soft-parts throughout the body. RT involving the central nervous system (CNS) is called atypical teratoid rhabdoid tumor (ATRT; see this term). (Orphanet Rare Disease Ontology, Orphanet_69077)
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1 genes associated with the Rhabdoid Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.