Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2015. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 292789016 | Congenital adrenogenital syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 574099017 | Congenital adrenogenital syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 76191000077116 | hyperplasie corticosurrénale congénitale | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| hyperplasie corticosurrénale congénitale | Is a | Adrenogenital disorder | false | Inferred relationship | Some | ||
| hyperplasie corticosurrénale congénitale | Finding site | Adrenal structure | false | Inferred relationship | Some | ||
| hyperplasie corticosurrénale congénitale | Finding site | Entire endocrine gonad (body structure) | false | Inferred relationship | Some | ||
| hyperplasie corticosurrénale congénitale | Is a | Congenital disease (disorder) | false | Inferred relationship | Some | ||
| hyperplasie corticosurrénale congénitale | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Feminisation-adrenogenital syndrome | Is a | False | hyperplasie corticosurrénale congénitale | Inferred relationship | Some | |
| Virilisation-adrenogenital syndrome | Is a | False | hyperplasie corticosurrénale congénitale | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set (foundation metadata concept)
FHIR