Atypical teratoid rhabdoid tumor (ATRT) is a highly malignant central nervous system (CNS) rhabdoid tumor (RT) found almost exclusively in children. [ Orphanet:99966 ]
Synonyms: malignant brain rhabdoid tumour rhabdoid neoplasm of CNS malignant rhabdoid tumour of brain rhabdoid tumor of the CNS CNS rhabdoid tumour atypical teratoid/rhabdoid tumour (morphologic abnormality) rhabdoid tumour of central nervous system atypical teratoid/rhabdoid tumour (WHO grade IV) atypical teratoid/rhabdoid tumor (WHO grade IV) ATT/RHT malignant rhabdoid tumour of the brain primary malignant rhabdoid tumour of brain malignant rhabdoid tumor of brain primary malignant rhabdoid tumor of brain central nervous system rhabdoid tumor primary malignant brain rhabdoid tumor primary malignant rhabdoid tumor of the brain rhabdoid tumor of central nervous system malignant brain rhabdoid neoplasm primary malignant rhabdoid neoplasm of the brain rhabdoid neoplasm of the central nervous system primary malignant brain rhabdoid neoplasm rhabdoid tumour of the CNS primary malignant rhabdoid tumour of the brain AT/RT malignant rhabdoid tumor of the brain rhabdoid neoplasm of the CNS rhabdoid neoplasm of central nervous system malignant brain rhabdoid tumor central nervous system rhabdoid tumour malignant rhabdoid neoplasm of brain rhabdoid tumor of CNS rhabdoid tumour of CNS ATRT atypical teratoid/rhabdoid tumour malignant rhabdoid neoplasm of the brain rhabdoid tumour of the central nervous system atypical teratoid/rhabdoid tumor primary malignant brain rhabdoid tumour atypical teratoid/rhabdoid tumor (morphologic abnormality) central nervous system rhabdoid neoplasm CNS rhabdoid neoplasm rhabdoid tumor of the central nervous system CNS rhabdoid tumor primary malignant rhabdoid neoplasm of brain
Term information
- DOID:2129 (MONDO:equivalentTo)
- EFO:1002008 (MONDO:equivalentTo)
- ICDO:9508/3 (NCIT:C6906)
- UMLS:C1266184 (NCIT:C6906)
- ONCOTREE:ATRT (MONDO:equivalentTo)
- Orphanet:99966 (MONDO:equivalentTo)
- NCIT:C6906 (MONDO:equivalentTo)
- GARD:16926 (Orphanet:99966)
gard_rare, ordo_clinical_subtype, rare, nord_rare, orphanet_rare
http://linkedlifedata.com/resource/umls/id/C1266184
http://purl.obolibrary.org/obo/DOID_2129
http://www.orpha.net/ORDO/Orphanet_99966
http://purl.obolibrary.org/obo/NCIT_C6906