Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3447488013 | Autosomal dominant medullary cystic kidney disease without hyperuricemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3447489017 | Autosomal dominant medullary cystic kidney disease without hyperuricaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3447490014 | Medullary cystic kidney disease 1 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3636198011 | Mucin 1 related autosomal dominant tubulointerstitial kidney disease (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3636199015 | MUC1-related autosomal dominant tubulointerstitial kidney disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
3636200017 | Mucin 1 related autosomal dominant tubulointerstitial kidney disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
MUC1-related autosomal dominant tubulointerstitial kidney disease | Is a | Autosomal dominant tubulointerstitial kidney disease | true | Inferred relationship | Some | ||
MUC1-related autosomal dominant tubulointerstitial kidney disease | Associated morphology | Fibrocystic change | true | Inferred relationship | Some | 1 | |
MUC1-related autosomal dominant tubulointerstitial kidney disease | Finding site | Structure of medulla of kidney | 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