Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3437473018 | Aggressive fibromatosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3437474012 | Aggressive fibromatosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3437475013 | Desmoid type fibromatosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3437476014 | Desmoid tumor | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3437477017 | Desmoid tumour | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3773008016 | Desmoid fibromatosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3773009012 | Deep fibromatosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3437478010 | Desmoid tumor can occur in any part of the body: extra-abdominally (neck, shoulders, upper limbs, gluteal region), abdominally (originating from muscle fascia or the abdominal/chest wall), and more rarely intra-abdominally in the mesentery or retroperitoneum. Depending on the location of the tumor, symptoms may include pain, fever and functional impairment or loss of function of the organ involved. Desmoid tumor results from the proliferation of well-differentiated myofibroblasts. The exact etiopathogenetic mechanism is still unknown, but they seem to have a multi-factorial origin with hormonal and genetic factors being involved. Somatic mutations in the CTNNB1 gene (3q21) encoding beta-catenin have been found in about 85 % of sporadic cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3437479019 | Desmoid tumour can occur in any part of the body: extra-abdominally (neck, shoulders, upper limbs, gluteal region), abdominally (originating from muscle fascia or the abdominal/chest wall), and more rarely intra-abdominally in the mesentery or retroperitoneum. Depending on the location of the tumour, symptoms may include pain, fever and functional impairment or loss of function of the organ involved. Desmoid tumour results from the proliferation of well-differentiated myofibroblasts. The exact aetiopathogenetic mechanism is still unknown, but they seem to have a multi-factorial origin with hormonal and genetic factors being involved. Somatic mutations in the CTNNB1 gene (3q21) encoding beta-catenin have been found in about 85% of sporadic cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Aggressive fibromatosis (disorder) | Associated morphology | Aggressive fibromatosis | true | Inferred relationship | Some | 1 | |
| Aggressive fibromatosis (disorder) | Is a | Neoplastic disease of uncertain behavior | false | Inferred relationship | Some | ||
| Aggressive fibromatosis (disorder) | Is a | Fibromatosis (disorder) | true | Inferred relationship | Some | ||
| Aggressive fibromatosis (disorder) | Is a | Neoplasm of uncertain behavior of soft tissues | true | Inferred relationship | Some | ||
| Aggressive fibromatosis (disorder) | Finding site | Structure of soft tissue (body structure) | true | Inferred relationship | Some | 1 |
This concept is not in any reference sets
FHIR