Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3310254011 | Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3311717010 | Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Is a | Familial hypomagnesemia-hypercalciuria | false | Inferred relationship | Some | ||
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Is a | Hereditary disorder of the urinary system | false | Inferred relationship | Some | ||
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Finding site | Urinary system structure (body structure) | false | Inferred relationship | Some | 1 | |
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Is a | Anomaly of eye (disorder) | true | Inferred relationship | Some | ||
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Is a | Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis (disorder) | true | Inferred relationship | Some | ||
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Finding site | Eye structure | true | Inferred relationship | Some | 2 | |
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Finding site | Structure of parenchyma of kidney | true | Inferred relationship | Some | 1 | |
| Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder) | Associated morphology | Pathologic calcification | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR