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FHIR
© HL7.org
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Server Home |
FHIR Server FHIR Server 3.7.22-SNAPSHOT
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FHIR Version n/a
User: [n/a]
Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4536636017 | Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4536637014 | Transient congenital hypothyroidism due to dual oxidase 2 mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 7704421000241113 | hypothyroïdie congénitale transitoire due à une mutation du gène codant pour la dual oxydase 2 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 7704431000241110 | hypothyroïdie congénitale transitoire due à une mutation du gène codant pour la DUOX2 (dual oxydase 2) | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Is a | Congenital hypothyroidism | true | Inferred relationship | Some | ||
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Is a | Transient hypothyroidism | true | Inferred relationship | Some | ||
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 | |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Due to | Chromosomal disorder (disorder) | true | Inferred relationship | Some | 2 | |
| Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) | Clinical course | Transitory | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets