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 |
| 1015661000172112 | hypothyroïdie congénitale idiopathique | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 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 |
| 750991000241119 | hypothyroïdie congénitale idiopathique (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 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 |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| hypothyroïdie congénitale idiopathique | est un(e) (attribut) | Primary hypothyroidism (disorder) | true | Inferred relationship | Some | ||
| hypothyroïdie congénitale idiopathique | localisation d'une constatation (attribut) | structure de la thyroïde | true | Inferred relationship | Some | 1 | |
| hypothyroïdie congénitale idiopathique | est un(e) (attribut) | maladie idiopathique | true | Inferred relationship | Some | ||
| hypothyroïdie congénitale idiopathique | est un(e) (attribut) | Congenital hypothyroidism | true | Inferred relationship | Some | ||
| hypothyroïdie congénitale idiopathique | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| hypothyroïdie congénitale idiopathique | localisation d'une constatation (attribut) | structure de la thyroïde | false | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR