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rhabdoid tumor

Disease Summary
Associated Targets (5491)
Tbio

3874

Tdark

729

Tchem

645

Tclin

243


GARD Rare
Mondo Description An aggressive malignant embryonal neoplasm usually occurring during childhood. It is characterized by the presence of large cells with abundant cytoplasm, large eccentric nucleus, and a prominent nucleolus and it is associated with abnormalities of chromosome 22. It can arise from the central nervous system, kidney, and the soft tissues. The prognosis is poor.
Disease Ontology Description A childhood kidney neoplasm that is located in the in the kidney as well as other locations outside the kidneys such as the liver, muscle, heart, lung, soft tissues, skin, the central nervous system.
Mondo Term and Equivalent IDs
MONDO:0002728:  rhabdoid tumor
EFO:0005701: 
GARD:0007572: 
MESH:D018335: 
NCIT:C3808: 
ONCOTREE:MRT: 
Orphanet:69077: 
UMLS:C0206743: