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 |
| 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 | Entire term case sensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 1015661000172112 | hypothyroïdie congénitale idiopathique | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 948511000172118 | idiopathische congenitale hypothyreoïdie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 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 |
This concept is not in any reference sets
FHIR