Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3333987011 | Congenital central hypothyroidism (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3333988018 | Congenital central hypothyroidism | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital central hypothyroidism | Is a | Central hypothyroidism | true | Inferred relationship | Existential restriction modifier | ||
| Congenital central hypothyroidism | Is a | Congenital hypothyroidism | true | Inferred relationship | Existential restriction modifier | ||
| Congenital central hypothyroidism | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital central hypothyroidism | Finding site | Thyroid structure | false | Inferred relationship | Existential restriction modifier | 2 | |
| Congenital central hypothyroidism | Finding site | Thyroid structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency | Is a | True | Congenital central hypothyroidism | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR