Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 315420015 | Individual with marker heterochromatin | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 591075011 | Individual with marker heterochromatin (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Individual with marker heterochromatin | Is a | Balanced rearrangement and structural marker | true | Inferred relationship | Some | ||
| Individual with marker heterochromatin | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
| Individual with marker heterochromatin | Finding site | Chromosome structure | false | Inferred relationship | Some | 1 | |
| Individual with marker heterochromatin | Finding site | Chromosome structure | false | Inferred relationship | Some | 1 | |
| Individual with marker heterochromatin | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | ||
| Individual with marker heterochromatin | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Individual with marker heterochromatin | Associated morphology | Alteration of chromosome structure | false | Inferred relationship | Some | ||
| Individual with marker heterochromatin | Finding site | Chromosome structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR