Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 315421016 | Individual with autosomal fragile site | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 591076012 | Individual with autosomal fragile site (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2480241000052119 | individ med autosomal fragile site | 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 |
| individ med autosomal fragile site | Is a | Balanced rearrangement and structural marker (disorder) | true | Inferred relationship | Some | ||
| individ med autosomal fragile site | Associated morphology | Alteration of chromosome structure | false | Inferred relationship | Some | ||
| individ med autosomal fragile site | Occurrence | Congenital | false | Inferred relationship | Some | ||
| individ med autosomal fragile site | Finding site | Chromosome structure | false | Inferred relationship | Some | 1 | |
| individ med autosomal fragile site | Associated morphology | kongenital anomali | false | Inferred relationship | Some | 1 | |
| individ med autosomal fragile site | Associated morphology | kongenital anomali | false | Inferred relationship | Some | ||
| individ med autosomal fragile site | Finding site | Chromosome structure | false | Inferred relationship | Some | 1 | |
| individ med autosomal fragile site | Finding site | Chromosome structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR