Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 356509012 | Familial idiopathic hypercalciuria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 626679012 | Familial idiopathic hypercalciuria (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial idiopathic hypercalciuria | Is a | Hypercalciuria | true | Inferred relationship | Existential restriction modifier | ||
| Familial idiopathic hypercalciuria | Is a | Disorder of phosphate, calcium and vitamin D metabolism | false | Inferred relationship | Existential restriction modifier | ||
| Familial idiopathic hypercalciuria | Finding site | Urinary tract structure | false | Inferred relationship | Existential restriction modifier | ||
| Familial idiopathic hypercalciuria | Finding site | Urinary system structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Familial idiopathic hypercalciuria | Is a | Idiopathic disease | true | Inferred relationship | Existential restriction modifier | ||
| Familial idiopathic hypercalciuria | Is a | Familial disease | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Williams syndrome | Is a | False | Familial idiopathic hypercalciuria | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR