Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module
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 | SNOMED CT core module |
| 3307393013 | Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3307394019 | Familial non-immune hyperthyroidism | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3307395018 | Familial non-autoimmune autosomal dominant hyperthyroidism | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor | Due to | Thyroid hormone responsiveness defect | true | Inferred relationship | Existential restriction modifier | 2 | |
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor | Is a | Hyperthyroidism | true | Inferred relationship | Existential restriction modifier | ||
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Existential restriction modifier | ||
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor | Finding site | Thyroid structure | false | Inferred relationship | Existential restriction modifier | ||
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 1 | |
| Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor | Finding site | Thyroid structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR