Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1234464015 | Cone-rod retinal dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
133294010 | Progressive cone-rod dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
821476014 | Progressive cone-rod dystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4594938019 | A rare retinal dystrophy with characteristics of photophobia, progressive loss of visual acuity, nystagmus, visual field abnormalities, abnormal color vision, and psychophysical and electrophysiological evidence of abnormal cone function. Progressive cone dystrophy usually presents in childhood or early adult life, and patients tend to develop rod photoreceptor dysfunction in later life. | en | Definition | Active | Case sensitive | SNOMED CT core |
4594939010 | A rare retinal dystrophy with characteristics of photophobia, progressive loss of visual acuity, nystagmus, visual field abnormalities, abnormal colour vision, and psychophysical and electrophysiological evidence of abnormal cone function. Progressive cone dystrophy usually presents in childhood or early adult life, and patients tend to develop rod photoreceptor dysfunction in later life. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | Is a | False | Progressive cone-rod dystrophy | Inferred relationship | Some |
Reference Sets
Emergency department reference set
Australian emergency department reference set
NSW Emergency Department reference set
Clinical finding foundation reference set
Emergency department diagnosis reference set
Problem/Diagnosis reference set