Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3528306010 | Multicystic renal dysplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3528307018 | Multicystic dysplastic kidney | en | Synonym | Active | Case insensitive | SNOMED CT core |
3528308011 | Multicystic renal dysplasia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3528309015 | MCKD - Multicystic kidney disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
3528310013 | A congenital anomaly of the kidney and urinary tract in which one or both kidneys are large, distended by multiple cysts, and non-functional. Global prevalence is not known, but the unilateral form is the most frequent. The disorder frequently presents antenatally at routine ultrasound scan. Bilateral disease is considered a lethal entity and most pregnancies are terminated. The disorder results from disrupted nephrogenesis but the exact pathogenic mechanism is still unknown. Mutations in the HNF1B gene (17q12) are strongly associated with the development of this disease. Most cases are sporadic. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Unilateral multicystic renal dysplasia | Is a | True | Multicystic renal dysplasia | Inferred relationship | Some | |
Bilateral multicystic renal dysplasia | Is a | True | Multicystic renal dysplasia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set