Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3446856017 | Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3446857014 | Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3446858016 | Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3446859012 | Renal hypomagnesemia type 3 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3446860019 | Renal hypomagnesaemia type 3 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | Is a | Familial hypomagnesemia-hypercalciuria | true | Inferred relationship | Existential restriction modifier | ||
| Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | Is a | Nephrocalcinosis | true | Inferred relationship | Existential restriction modifier | ||
| Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | Is a | Hereditary nephropathy | true | Inferred relationship | Existential restriction modifier | ||
| Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | Associated morphology | Pathologic calcification, calcified structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | Finding site | Kidney structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR