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 |
| 3446282017 | Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3446283010 | Infundibulopelvic stenosis multicystic kidney syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3446284016 | Infundibulopelvic dysgenesis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 761801000241118 | syndrome de dysplasie rénale autosomique dominante-sténose infundibulo-pelvienne (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 913061000172113 | syndrome de dysplasie rénale autosomique dominante-sténose infundibulo-pelvienne | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3446285015 | A rare genetic renal malformation syndrome with characteristics of variable degrees of malformation in the pelvicalyceal system (including unilateral or bilateral calyceal dilatation, infundibular stenosis, hypoplasia or stenosis of the renal pelvis) which lead to multicystic kidney. Clinically it exhibits abdominal, lumbar or flank pain, recurrent urinary tract infections, hypertension, proteinuria and often progresses to renal insufficiency. Calyceal dilatation and hydronephrosis are frequently seen on imaging. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | morphologie associée (attribut) | structure anormale sur le plan morphologique | true | Inferred relationship | Some | 1 | |
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | est un(e) (attribut) | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | est un(e) (attribut) | anomalie congénitale des reins | true | Inferred relationship | Some | ||
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | est un(e) (attribut) | Congenital anomaly of the urinary tract proper (disorder) | true | Inferred relationship | Some | ||
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | est un(e) (attribut) | Hereditary nephropathy (disorder) | true | Inferred relationship | Some | ||
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | morphologie associée (attribut) | Developmental abnormality | false | Inferred relationship | Some | 1 | |
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | localisation d'une constatation (attribut) | Renal collecting system structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR