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 |
| 434881000241114 | néphrocalcinose (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 50007131000188118 | néphrocalcinose | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 786228017 | Nephrocalcinosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 81047018 | Nephrocalcinosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| syndrome amélogenèse imparfaite-néphrocalcinose | est un(e) (attribut) | True | néphrocalcinose (trouble) | Inferred relationship | Some | |
| Neonatal nephrocalcinosis | est un(e) (attribut) | True | néphrocalcinose (trouble) | Inferred relationship | Some | |
| Microscopic nephrocalcinosis | est un(e) (attribut) | True | néphrocalcinose (trouble) | Inferred relationship | Some | |
| Macroscopic nephrocalcinosis | est un(e) (attribut) | True | néphrocalcinose (trouble) | Inferred relationship | Some | |
| Bartter's syndrome with hypercalciuria and nephrocalcinosis | est un(e) (attribut) | False | néphrocalcinose (trouble) | Inferred relationship | Some | |
| Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder) | est un(e) (attribut) | True | néphrocalcinose (trouble) | Inferred relationship | Some |
Reference Sets
FHIR