Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3444866010 | Hereditary skin fragility (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3444867018 | Hereditary skin fragility | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3444868011 | Genetically determined skin fragility | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary skin fragility | Is a | Disorder of skin | true | Inferred relationship | Some | ||
| Hereditary skin fragility | Is a | Fragile skin | true | Inferred relationship | Some | ||
| Hereditary skin fragility | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| Hereditary skin fragility | Finding site | Skin structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Bullous ichthyosiform erythroderma | Is a | True | Hereditary skin fragility | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR