Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 81047018 | Nephrocalcinosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 786228017 | Nephrocalcinosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 50007131000188118 | néphrocalcinose | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Microscopic nephrocalcinosis | Is a | True | Nephrocalcinosis | Inferred relationship | Some | |
| Macroscopic nephrocalcinosis (disorder) | Is a | True | Nephrocalcinosis | Inferred relationship | Some | |
| Neonatal nephrocalcinosis | Is a | True | Nephrocalcinosis | Inferred relationship | Some | |
| Bartter's syndrome with hypercalciuria and nephrocalcinosis | Is a | False | Nephrocalcinosis | Inferred relationship | Some | |
| Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder) | Is a | True | Nephrocalcinosis | Inferred relationship | Some | |
| Enamel-renal syndrome | Is a | True | Nephrocalcinosis | Inferred relationship | Some | |
| Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome (disorder) | Is a | True | Nephrocalcinosis | Inferred relationship | Some |
This concept is not in any reference sets
FHIR