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
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Term information
database
cross reference
- 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))
- OMIM:609322 (BTNT (ORPHA code's Broader Term maps to a Narrower Term))
definition citation
- Orphanet
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 cases/families value
- 500.0
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: