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 |
| 3326183011 | Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3326184017 | Hyperinsulinism due to uncoupling protein 2 deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3326185016 | Hyperinsulinism due to UCP2 deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3326186015 | Hyperinsulinism due to UCP2 (uncoupling protein 2) deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3326187012 | A form of diazoxide-sensitive diffuse hyperinsulinism characterized by hypoglycemic episodes from the neonatal period, a good clinical response to diazoxide and a probable transient nature of the disease with spontaneous resolution. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3326188019 | A form of diazoxide-sensitive diffuse hyperinsulinism characterised by hypoglycaemic episodes from the neonatal period, a good clinical response to diazoxide and a probable transient nature of the disease with spontaneous resolution. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) | est un(e) (attribut) | Congenital disease | true | Inferred relationship | Some | ||
| Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) | est un(e) (attribut) | Hyperinsulinism | true | Inferred relationship | Some | ||
| Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) | est un(e) (attribut) | Digestive system hereditary disorder | true | Inferred relationship | Some | ||
| Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) | est un(e) (attribut) | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) | localisation d'une constatation (attribut) | structure du pancréas endocrine | false | Inferred relationship | Some | ||
| Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) | localisation d'une constatation (attribut) | structure du pancréas endocrine | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR