Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4213324014 | Usher syndrome type 3 | en | Synonym | Active | Case sensitive | SNOMED CT core |
4279326016 | Retinitis pigmentosa-deafness syndrome type 3 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4279327013 | Retinitis pigmentosa-deafness syndrome type 3 | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Retinitis pigmentosa-deafness syndrome type 3 | Is a | Retinitis pigmentosa-deafness syndrome | true | Inferred relationship | Some | ||
Retinitis pigmentosa-deafness syndrome type 3 | Finding site | Structure of auditory system | true | Inferred relationship | Some | 1 | |
Retinitis pigmentosa-deafness syndrome type 3 | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Retinitis pigmentosa-deafness syndrome type 3 | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 2 | |
Retinitis pigmentosa-deafness syndrome type 3 | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Retinitis pigmentosa-deafness syndrome type 3 | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Retinitis pigmentosa-deafness syndrome type 3 | Interprets | Hearing | true | Inferred relationship | Some | 3 | |
Retinitis pigmentosa-deafness syndrome type 3 | Finding site | Retinal structure | true | Inferred relationship | Some | 4 | |
Retinitis pigmentosa-deafness syndrome type 3 | Associated morphology | Dystrophy | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set