Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4009842013 | Foetal acitretin syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4009844014 | Acitretin embryofoetopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4009845010 | Acitretin embryopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4009846011 | Fetal acitretin syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4009847019 | Acitretin embryofetopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4013006018 | Embryopathy caused by acitretin (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4013007010 | Embryopathy caused by acitretin | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Embryopathy caused by acitretin | Is a | Embryopathy caused by retinoid | true | Inferred relationship | Existential restriction modifier | ||
| Embryopathy caused by acitretin | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Embryopathy caused by acitretin | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Embryopathy caused by acitretin | Causative agent | Acitretin | true | Inferred relationship | Existential restriction modifier | 1 | |
| Embryopathy caused by acitretin | Occurrence | Fetal period | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR