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. [ NCIT:C3808 ]
Synonyms: rhabdoid sarcoma malignant rhabdoid tumor rhabdoid tumor malignant rhabdoid tumour
Term information
- UMLS:C0206743 (Orphanet:69077/e)
- GARD:7572 (Orphanet:69077)
- DOID:3672 (MONDO:equivalentTo)
- ICDO:8963/3 (NCIT:C3808)
- NCIT:C3808 (MONDO:equivalentTo)
- Orphanet:69077 (MONDO:equivalentTo)
- ONCOTREE:MRT (MONDO:equivalentTo)
- EFO:0005701 (MONDO:equivalentTo)
- MESH:D018335 (Orphanet:69077/e)
gard_rare, ordo_disease, rare, nord_rare, orphanet_rare
http://linkedlifedata.com/resource/umls/id/C0206743
http://purl.obolibrary.org/obo/NCIT_C3808
http://identifiers.org/mesh/D018335
http://www.orpha.net/ORDO/Orphanet_69077
http://purl.obolibrary.org/obo/DOID_3672