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 |
3447485011 | Autosomal dominant medullary cystic kidney disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3636201018 | Autosomal dominant tubulointerstitial kidney disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3636202013 | Autosomal dominant tubulointerstitial kidney disease (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403514018 | A rare, genetic renal tubular disease characterized by tubular damage and interstitial fibrosis in absence of glomerular lesions and clinically manifesting with chronic kidney disease (CKD) and slow progression to end-stage kidney disease (ESKD). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403515017 | A rare, genetic renal tubular disease characterised by tubular damage and interstitial fibrosis in absence of glomerular lesions and clinically manifesting with chronic kidney disease (CKD) and slow progression to end-stage kidney disease (ESKD). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant tubulointerstitial kidney disease | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant tubulointerstitial kidney disease | Is a | Medullary cystic disease of the kidney | true | Inferred relationship | Some | ||
Autosomal dominant tubulointerstitial kidney disease | Is a | Hereditary nephropathy (disorder) | true | Inferred relationship | Some | ||
Autosomal dominant tubulointerstitial kidney disease | Associated morphology | Fibrocystic change | true | Inferred relationship | Some | 1 | |
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 |
UMOD-related autosomal dominant tubulointerstitial kidney disease | Is a | True | Autosomal dominant tubulointerstitial kidney disease | Inferred relationship | Some | |
Mucin 1 related autosomal dominant tubulointerstitial kidney disease (disorder) | Is a | True | Autosomal dominant tubulointerstitial kidney disease | Inferred relationship | Some |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)