Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
354466018 | Acquired Fanconi syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
354467010 | Secondary Fanconi syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
625064013 | Acquired Fanconi syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
6002211000241113 | syndrome de Fanconi acquis | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Acquired Fanconi syndrome | Is a | Infantile nephropathic cystinosis | false | Inferred relationship | Some | ||
Acquired Fanconi syndrome | Occurrence | Congenital | false | Inferred relationship | Some | ||
Acquired Fanconi syndrome | Associated morphology | inflammation | false | Inferred relationship | Some | ||
Acquired Fanconi syndrome | Finding site | Structure of interstitial tissue of kidney | false | Inferred relationship | Some | ||
Acquired Fanconi syndrome | Is a | Proximal renal tubular acidosis | true | Inferred relationship | Some | ||
Acquired Fanconi syndrome | Finding site | Kidney structure | false | Inferred relationship | Some | ||
Acquired Fanconi syndrome | Occurrence | Any period of life commencing after birth, but before death. | true | Inferred relationship | Some | 1 | |
Acquired Fanconi syndrome | Finding site | Proximal convoluted renal tubule structure | true | Inferred relationship | Some | 1 | |
Acquired Fanconi syndrome | Is a | Fanconi syndrome | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Adult Fanconi syndrome | Is a | True | Acquired Fanconi syndrome | Inferred relationship | Some | |
A rare monoclonal gammopathy characterized by renal proximal tubule dysfunction secondary to monoclonal kappa light chain deposits in proximal tubular cells. Clinical presentation is with variable chronic kidney disease, low molecular weight proteinuria, aminoaciduria, hyperphosphaturia, uricosuria, bicarbonaturia, and non-diabetic glycosuria. Renal phosphate and urate wasting may cause hypophosphatemia and hypouricemia. | Is a | False | Acquired Fanconi syndrome | Inferred relationship | Some |
This concept is not in any reference sets