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 |
| 3307392015 | Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3307393013 | Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3307394019 | Familial non-immune hyperthyroidism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3307395018 | Familial non-autoimmune autosomal dominant hyperthyroidism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3307396017 | A rare hyperthyroidism characterized by mild to severe hyperthyroidism, presence of goiter, absence of features of autoimmunity, frequent relapses while on treatment and a positive family history. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3307397014 | A rare hyperthyroidism characterised by mild to severe hyperthyroidism, presence of goitre, absence of features of autoimmunity, frequent relapses while on treatment and a positive family history. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4338601000052113 | familjär icke-autoimmun autosomal dominant hypertyreos | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder) | Due to | Thyroid hormone responsiveness defect | true | Inferred relationship | Some | 2 | |
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder) | Is a | Hyperthyroidism | true | Inferred relationship | Some | ||
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder) | Finding site | Thyroid structure | false | Inferred relationship | Some | ||
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (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