Status: current, Primitive. 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 | Case insensitive | SNOMED CT core |
3309082013 | Idiopathic congenital hypothyroidism | en | Synonym | Active | Case insensitive | SNOMED CT core |
3309083015 | Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause and prevalence are unknown. Clinical manifestations are those of other forms of congenital hypothyroidism. Goiter is always absent. Ultrasound examination and thyroid scintigraphy show a thyroid gland of normal shape and size in the normal, eutopic location. Idiopathic congenital hypothyroidism can be diagnosed after exclusion of the known causes of congenital hypothyroidism. | en | Definition | Active | Case sensitive | SNOMED CT core |
3309084014 | Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause and prevalence are unknown. Clinical manifestations are those of other forms of congenital hypothyroidism. Goitre is always absent. Ultrasound examination and thyroid scintigraphy show a thyroid gland of normal shape and size in the normal, eutopic location. Idiopathic congenital hypothyroidism can be diagnosed after exclusion of the known causes of congenital hypothyroidism. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Idiopathic congenital hypothyroidism | Is a | Primary hypothyroidism | true | Inferred relationship | Some | ||
Idiopathic congenital hypothyroidism | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 | |
Idiopathic congenital hypothyroidism | Is a | Idiopathic disease | true | Inferred relationship | Some | ||
Idiopathic congenital hypothyroidism | Is a | Congenital hypothyroidism | true | Inferred relationship | Some | ||
Idiopathic congenital hypothyroidism | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Idiopathic congenital hypothyroidism | Finding site | Thyroid structure | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set