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 |
| 1019221000172115 | méga-uretère primitif congénital | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3309412012 | Congenital primary megaureter (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3309413019 | Congenital primary megaureter | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3309414013 | Congenital primary megalo-ureter | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 751081000241114 | méga-uretère primitif congénital (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3309415014 | An idiopathic condition in which the bladder and bladder outlet are normal but the ureter is dilated to some extent. It may be obstructed, refluxing or unobstructed and not refluxing. Prevalence is unknown, but is the second most common cause of neonatal hydronephrosis. About half of cases are asymptomatic and are discovered on routine antenatal ultrasound. The cause is unknown but it may be due to high fetal urine outflow, changes in the ureter pre and postnatal or transient anatomical obstructions that improve with postnatal development, such as ureteral folds. Not known to be hereditary, but families with more than one affected member have been described. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| méga-uretère primitif congénital | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| méga-uretère primitif congénital | morphologie associée (attribut) | dilatation | true | Inferred relationship | Some | 1 | |
| méga-uretère primitif congénital | est un(e) (attribut) | Idiopathic dilation of ureter | true | Inferred relationship | Some | ||
| méga-uretère primitif congénital | est un(e) (attribut) | Congenital dilatation of ureter (disorder) | true | Inferred relationship | Some | ||
| méga-uretère primitif congénital | morphologie associée (attribut) | Congenital dilatation (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| méga-uretère primitif congénital | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| méga-uretère primitif congénital | localisation d'une constatation (attribut) | uretère (structure corporelle) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR