Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3310271012 | Familial primary hypomagnesemia with normocalciuria (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3310272017 | Familial primary hypomagnesemia with normocalciuria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3311715019 | Familial primary hypomagnesaemia with normocalciuria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial primary hypomagnesemia with normocalciuria | Is a | Autosomal hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Familial primary hypomagnesemia with normocalciuria | Is a | Primary hypomagnesemia | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial primary hypomagnesemia with normocalciuria and normocalcemia | Is a | True | Familial primary hypomagnesemia with normocalciuria | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR