Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3310253017 | Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3310254011 | Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3311717010 | Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement | Is a | Familial hypomagnesaemia-hypercalciuria | true | Inferred relationship | Some | ||
| Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement | Is a | Hereditary disorder of the urinary system | true | Inferred relationship | Some | ||
| Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement | Finding site | Urinary system structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set