Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1230469015 | Carrier of genetic disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
494838011 | Genetic disorder carrier | en | Synonym | Active | Case insensitive | SNOMED CT core |
784922010 | Genetic disorder carrier (finding) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Genetic disorder carrier | Is a | Carrier of disorder | true | Inferred relationship | Some | ||
Genetic disorder carrier | Is a | Baby miscellaneous "at-risk" factors | false | Inferred relationship | Some | ||
Genetic disorder carrier | Is a | Context-dependent finding | false | Inferred relationship | Some | ||
Genetic disorder carrier | Is a | Finding of lesion | false | Inferred relationship | Some | ||
Genetic disorder carrier | Interprets | General clinical state | true | Inferred relationship | Some | 1 | |
Genetic disorder carrier | Associated morphology | Congenital anomaly | false | Inferred relationship | Some |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set