Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
119538012 | Hypercalciuria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
812159017 | Hypercalciuria (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
1233435015 | Hypercalcuria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hypercalciuria | Is a | Disorder of calcium metabolism | true | Inferred relationship | Existential restriction modifier | ||
Hypercalciuria | Is a | Symptomatic disorders of the urinary tract | true | Inferred relationship | Existential restriction modifier | ||
Hypercalciuria | Finding site | Urinary tract structure | false | Inferred relationship | Existential restriction modifier | ||
Hypercalciuria | Finding site | Urinary system structure | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial idiopathic hypercalciuria | Is a | True | Hypercalciuria | Inferred relationship | Existential restriction modifier | |
Familial hypomagnesemia-hypercalciuria | Is a | True | Hypercalciuria | Inferred relationship | Existential restriction modifier | |
Bartter's syndrome with hypercalciuria and nephrocalcinosis | Is a | False | Hypercalciuria | Inferred relationship | Existential restriction modifier | |
Hereditary hypophosphatemic rickets with hypercalciuria | Is a | True | Hypercalciuria | Inferred relationship | Existential restriction modifier | |
Bartter syndrome | Is a | True | Hypercalciuria | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets