Status: current, Defined. Date: 31-Jul 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3897143012 | Congenital generalized hypertrichosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3897144018 | Congenital generalised hypertrichosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3897145017 | Congenital generalized hypertrichosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital generalised hypertrichosis | Is a | Lanugo | true | Inferred relationship | Some | ||
Congenital generalised hypertrichosis | Is a | Congenital hypertrichosis | true | Inferred relationship | Some | ||
Congenital generalised hypertrichosis | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital generalised hypertrichosis | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital generalised hypertrichosis | Associated morphology | Growth alteration | true | Inferred relationship | Some | 1 | |
Congenital generalised hypertrichosis | Finding site | Lanugo hair | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
X-linked congenital generalised hypertrichosis | Is a | True | Congenital generalised hypertrichosis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set