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 |
| 6946641000146112 | syndroom van infundibulopelvisstenose en multicysteuze nier | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6946651000146110 | syndroom van infundibulopelvisstenose en multicysteuze nier (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained 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) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | Is a | Congenital anomaly of the kidney | true | Inferred relationship | Some | ||
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | Is a | Congenital anomaly of the urinary tract proper (disorder) | true | Inferred relationship | Some | ||
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | Is a | Hereditary nephropathy (disorder) | true | Inferred relationship | Some | ||
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | Associated morphology | gebrekkige ontwikkeling (afwijkende morfologie) | false | Inferred relationship | Some | 1 | |
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | Finding site | Renal collecting system structure | true | Inferred relationship | Some | 1 | |
| Infundibulopelvic stenosis multicystic kidney syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | 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) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
FHIR