Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
119538012 | Hypercalciuria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
812159017 | Hypercalciuria (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1233435015 | Hypercalcuria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hypercalciuria | Is a | Disorder of calcium metabolism | true | Inferred relationship | Some | ||
Hypercalciuria | Is a | Symptomatic disorders of the urinary tract | false | Inferred relationship | Some | ||
Hypercalciuria | Finding site | Urinary tract structure | false | Inferred relationship | Some | ||
Hypercalciuria | Finding site | Urinary tract includes entire kidney and the urinary tract proper which relate to the ureter, bladder and urethra. | true | Inferred relationship | Some | 1 | |
Hypercalciuria | Is a | Urine calcium above reference range (finding) | true | Inferred relationship | Some | ||
Hypercalciuria | Is a | Disorder of urinary system (disorder) | true | Inferred relationship | Some | ||
Hypercalciuria | Interprets | Calcium measurement, urine | true | Inferred relationship | Some | 2 | |
Hypercalciuria | Has interpretation | Above reference range | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial idiopathic hypercalciuria | Is a | True | Hypercalciuria | Inferred relationship | Some | |
Familial hypomagnesemia-hypercalciuria | Is a | True | Hypercalciuria | Inferred relationship | Some | |
Bartter's syndrome with hypercalciuria and nephrocalcinosis | Is a | False | Hypercalciuria | Inferred relationship | Some | |
A rare hereditary disorder of renal phosphate wasting characterized by hypophosphatemia and hypercalciuria associated with rickets and/or osteomalacia. Other features include slow growth, short stature, skeletal deformities, muscle weakness and bone pain that are associated with normal or elevated plasma levels of calcitriol and hyperphosphaturia. | Is a | True | Hypercalciuria | Inferred relationship | Some | |
Bartter syndrome (disorder) | Is a | True | Hypercalciuria | Inferred relationship | Some |
This concept is not in any reference sets