Status: current, Primitive. 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 | Case insensitive | SNOMED CT core |
3446283010 | Infundibulopelvic stenosis multicystic kidney syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3446284016 | Infundibulopelvic dysgenesis | en | Synonym | Active | Case insensitive | SNOMED CT core |
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 | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Infundibulopelvic stenosis multicystic kidney syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
Infundibulopelvic stenosis multicystic kidney syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Infundibulopelvic stenosis multicystic kidney syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Infundibulopelvic stenosis multicystic kidney syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Infundibulopelvic stenosis multicystic kidney syndrome | Is a | Congenital anomaly of the kidney | true | Inferred relationship | Some | ||
Infundibulopelvic stenosis multicystic kidney syndrome | Is a | Congenital anomaly of the urinary tract proper | true | Inferred relationship | Some | ||
Infundibulopelvic stenosis multicystic kidney syndrome | Is a | Hereditary nephropathy | true | Inferred relationship | Some | ||
Infundibulopelvic stenosis multicystic kidney syndrome | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 | |
Infundibulopelvic stenosis multicystic kidney syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Infundibulopelvic stenosis multicystic kidney syndrome | Finding site | Renal collecting system structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set