Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4574263015 | DSRCT - desmoplastic small round cell tumour | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4574264014 | DSRCT - desmoplastic small round cell tumor | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4574265010 | Desmoplastic small round cell tumor (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4574266011 | Desmoplastic small round cell tumour | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4574267019 | Desmoplastic small round cell tumor | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4574261018 | An aggressive soft tissue cancer that typically arises in serous lined surfaces of the abdominal or pelvic peritoneum, and spreads to the omentum, lymph nodes and hematogenously disseminates especially to the liver. Extraserous primary location has been reported in exceptional cases. The disease appears to originate from the mesothelium. In almost all cases, a specific translocation t(11;22)(p13;q12) is found that juxtaposes the EWSR1 gene to the WT1 tumor suppressor gene. However, the underlying molecular mechanism remains unknown. Several other associated chromosomal translocations have been described (t(5;19), t(X;16) and t(4;10)). Prognosis is poor. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4574262013 | An aggressive soft tissue cancer that typically arises in serous lined surfaces of the abdominal or pelvic peritoneum, and spreads to the omentum, lymph nodes and haematogenously disseminates especially to the liver. Extraserous primary location has been reported in exceptional cases. The disease appears to originate from the mesothelium. In almost all cases, a specific translocation t(11;22)(p13;q12) is found that juxtaposes the EWSR1 gene to the WT1 tumour suppressor gene. However, the underlying molecular mechanism remains unknown. Several other associated chromosomal translocations have been described (t(5;19), t(X;16) and t(4;10)). Prognosis is poor. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5088631000052118 | desmoplastisk smårundcellig tumör | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Desmoplastic small round cell tumor (disorder) | Associated morphology | Desmoplastic small round cell tumor | true | Inferred relationship | Some | 1 | |
| Desmoplastic small round cell tumor (disorder) | Is a | Primary malignant neoplasm of soft tissues (disorder) | true | Inferred relationship | Some | ||
| Desmoplastic small round cell tumor (disorder) | Finding site | Structure of soft tissue (body structure) | true | Inferred relationship | Some | 1 | |
| Desmoplastic small round cell tumor (disorder) | Is a | Sarcoma of soft tissue (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR