Status: current, Not 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 | Reference Sets |
| 3424453012 | Embryopathy caused by mycophenolate mofetil (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
| 3424454018 | Embryopathy caused by mycophenolate mofetil | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | GB English: Acceptable (foundation metadata concept) |
| 3424455017 | Mycophenolate mofetil embryopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
| 3424456016 | A malformative syndrome due to the teratogenic effect of mycophenolate mofetil (MMF), an effective immunosuppressive agent widely used for the prevention of organ rejection after organ transplantation. To date the majority of cases have been offspring of women who received a solid organ transplant. The newborn or fetus generally has external ear anomalies. Cleft lip-palate with micrognathia is frequently observed. Aberrant orofacial cleft has been observed in one case. Ocular anomalies, such as microphthalmia and iris or chorioretinal coloboma are also frequent. Distal limbs anomalies as well as congenital malformations of the heart, kidneys and/or central nervous system may also be observed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
| 3978421000052110 | embryopati orsakad av mykofenolatmofetil | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) | Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Embryopathy caused by mycophenolate mofetil (disorder) | Is a | Drug-related disorder | true | Inferred relationship | Some | ||
| Embryopathy caused by mycophenolate mofetil (disorder) | Is a | medfött missbildningssyndrom orsakat av känd exogen faktor | false | Inferred relationship | Some | ||
| Embryopathy caused by mycophenolate mofetil (disorder) | Is a | Disorder of fetal structure | false | Inferred relationship | Some | ||
| Embryopathy caused by mycophenolate mofetil (disorder) | Associated morphology | Developmental anomaly (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| Embryopathy caused by mycophenolate mofetil (disorder) | Causative agent | Mycophenolate mofetil (substance) | true | Inferred relationship | Some | 1 | |
| Embryopathy caused by mycophenolate mofetil (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Embryopathy caused by mycophenolate mofetil (disorder) | Finding site | Fetal structure | true | Inferred relationship | Some | 1 | |
| Embryopathy caused by mycophenolate mofetil (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Embryopathy caused by mycophenolate mofetil (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Embryopathy caused by mycophenolate mofetil (disorder) | Is a | Congenital malformation syndrome (disorder) | true | Inferred relationship | Some | ||
| Embryopathy caused by mycophenolate mofetil (disorder) | Is a | Disorder by body site (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR