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
- OMIM:609322 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- UMLS:C0206743 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:C49.9 (- NTBT (ORPHA code's Narrower Term maps to a Broader Term). - Attributed (The ICD10 code is attributed by Orphanet).)
- OMIM:613325 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
- MeSH:D018335 (E (Exact mapping: the two concepts are equivalent))
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