Status: current, Defined. Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
347705019 | X-linked retinitis pigmentosa | en | Synonym | Active | Case sensitive | SNOMED CT core |
620069017 | X-linked retinitis pigmentosa (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
X-linked retinitis pigmentosa | Is a | X-linked hereditary disease | true | Inferred relationship | Some | ||
X-linked retinitis pigmentosa | Is a | Retinitis pigmentosa | true | Inferred relationship | Some | ||
X-linked retinitis pigmentosa | Finding site | Retinal structure | false | Inferred relationship | Some | ||
X-linked retinitis pigmentosa | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
X-linked retinitis pigmentosa | Finding site | Retinal structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Chromosome Xp11.3 microdeletion syndrome | Is a | True | X-linked retinitis pigmentosa | Inferred relationship | Some | |
X-linked retinitis pigmentosa heterozygote | Is a | True | X-linked retinitis pigmentosa | Inferred relationship | Some | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome | Is a | True | X-linked retinitis pigmentosa | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set