Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5408598018 | A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5408599014 | A rare, genetic renal tubular disease characterised by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3759533019 | Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3759536010 | Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3759537018 | Dominant hypophosphataemia with nephrolithiasis and/or osteoporosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5591721000241115 | hypophosphatémie dominante avec néphrolithiase et/ou ostéoporose | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3440391001000112 | Dominante Hypophosphatämie mit Nephrolithiasis oder Osteoporose | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Finding site | Osteoid tissue | true | Inferred relationship | Some | 1 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Is a | Hereditary nephropathy (disorder) | true | Inferred relationship | Some | ||
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Is a | Renal tubular disorder | true | Inferred relationship | Some | ||
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Is a | Autosomal dominant hypophosphataemic bone disease | true | Inferred relationship | Some | ||
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Due to | Specific renal tubule transport defect | false | Inferred relationship | Some | 3 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Finding site | Renal tubule structure | false | Inferred relationship | Some | 2 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 4 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Associated morphology | Impaired mineralization | false | Inferred relationship | Some | 4 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Finding site | Bone structure | false | Inferred relationship | Some | 4 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Associated morphology | Impaired mineralization | true | Inferred relationship | Some | 2 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Finding site | Bone structure | true | Inferred relationship | Some | 2 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Finding site | Renal tubule structure | true | Inferred relationship | Some | 3 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Due to | Specific renal tubule transport defect | true | Inferred relationship | Some | 4 | |
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Is a | Urinary complication | true | Inferred relationship | Some | ||
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. | Is a | Metabolic renal disease | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)