Status: current, Defined. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2722977018 | Pancreatoblastoma (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 291682019 | Pancreatoblastoma | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4574184017 | A rare neoplastic gastroenterologic disease most often found in children, which usually presents with the non-specific symptoms of a palpable mass, vomiting, abdominal pain, jaundice, and weight loss/failure to thrive. Histologically, this malignant epithelial pancreatic neoplasm of the exocrine cells has multiple lines of differentiation (acinar, ductal, mesenchymal, neuroendocrine) and the presence of squamoid nests. Pancreatoblastoma can occur in any part of the pancreas. It is a malignant embryonal neoplasm that seems to recapitulate the embryogenesis of the pancreas, presumably because it originates from the pluripotent pancreatic stem cells during foregut development. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Pancreatoblastoma | Finding site | Pancreatic structure | true | Inferred relationship | Some | 1 | |
| Pancreatoblastoma | Is a | Primary malignant neoplasm of pancreas | false | Inferred relationship | Some | ||
| Pancreatoblastoma | Associated morphology | Pancreatoblastoma | true | Inferred relationship | Some | 1 | |
| Pancreatoblastoma | Is a | Malignant tumour of pancreas | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set
FHIR