Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3309081018 | Idiopathic congenital hypothyroidism (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3309082013 | Idiopathic congenital hypothyroidism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401564016 | Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause and prevalence are unknown. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Idiopathic congenital hypothyroidism (disorder) | Is a | Idiopathic disease | true | Inferred relationship | Some | ||
Idiopathic congenital hypothyroidism (disorder) | Is a | Congenital hypothyroidism | true | Inferred relationship | Some | ||
Idiopathic congenital hypothyroidism (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Idiopathic congenital hypothyroidism (disorder) | Finding site | Thyroid structure | false | Inferred relationship | Some | 2 | |
Idiopathic congenital hypothyroidism (disorder) | Is a | Primary hypothyroidism | true | Inferred relationship | Some | ||
Idiopathic congenital hypothyroidism (disorder) | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)