Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3307131017 | Severe early childhood onset retinal dystrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3307132012 | Severe early childhood onset retinal dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3307135014 | SECORD - Severe early childhood onset retinal dystrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3307136010 | An inherited retinal dystrophy with manifestation of severe congenital night blindness, progressive retinal dystrophy and nystagmus. Blindness is often complete by the age of 30 years. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Severe early childhood onset retinal dystrophy | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Some | ||
| Severe early childhood onset retinal dystrophy | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Severe early childhood onset retinal dystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
| Severe early childhood onset retinal dystrophy | Occurrence | Early childhood | true | Inferred relationship | Some | 1 | |
| Severe early childhood onset retinal dystrophy | Finding site | Retinal structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Unit of use quantity reference set
Description inactivation indicator reference set