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).

Synonyms: Malignant rhabdoid tumor

This is just here as a test because I lose it

Term information

database cross reference
expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=69077

hasDbXref

OMIM:613325

ICD-10:C49.9

UMLS:C0206743

OMIM:609322

MeSH:D018335

has age of onset

http://www.orpha.net/ORDO/Orphanet_409946

http://www.orpha.net/ORDO/Orphanet_409945

http://www.orpha.net/ORDO/Orphanet_409944

http://www.orpha.net/ORDO/Orphanet_409943

has annual incidence range

http://www.orpha.net/ORDO/Orphanet_409979

has inheritance

http://www.orpha.net/ORDO/Orphanet_409941

has point prevalence range

http://www.orpha.net/ORDO/Orphanet_409981

notation

ORPHA:69077

part of

http://www.orpha.net/ORDO/Orphanet_3394

present in

http://www.orpha.net/ORDO/Orphanet_409991

http://www.orpha.net/ORDO/Orphanet_409984

Term relations

Subclass of: