Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3302597019 | Fetal indomethacin syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302598012 | Foetal indomethacin syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302602014 | Embryofetopathy caused by indomethacin (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302603016 | Embryofetopathy caused by indomethacin | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302622013 | Indomethacin embryofetopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302600018 | A group of symptoms which may be observed in the fetus or newborn when the mother has taken indomethacin, a nonsteroidal anti-inflammatory drug during pregnancy. The drug crosses the human placenta readily throughout gestation, but its effects on the embryo/fetus vary according to the stage of pregnancy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Embryofetopathy caused by indomethacin (disorder) | Is a | Drug-related disorder | false | Inferred relationship | Some | ||
| Embryofetopathy caused by indomethacin (disorder) | Is a | Congenital malformation syndrome due to known exogenous cause | false | Inferred relationship | Some | ||
| Embryofetopathy caused by indomethacin (disorder) | Is a | Disorder of fetal structure | false | Inferred relationship | Some | ||
| Embryofetopathy caused by indomethacin (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 1 | |
| Embryofetopathy caused by indomethacin (disorder) | Causative agent | Indometacin | true | Inferred relationship | Some | 1 | |
| Embryofetopathy caused by indomethacin (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Embryofetopathy caused by indomethacin (disorder) | Finding site | Fetal structure | true | Inferred relationship | Some | 1 | |
| Embryofetopathy caused by indomethacin (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Embryofetopathy caused by indomethacin (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Embryofetopathy caused by indomethacin (disorder) | Is a | Congenital malformation syndrome (disorder) | true | Inferred relationship | Some | ||
| Embryofetopathy caused by indomethacin (disorder) | Is a | Disorder by body site | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR