Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4696045016 | Familial cavitary optic disc anomaly (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4696046015 | Familial CODA (cavitary optic disc anomaly) | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4696047012 | Familial cavitary optic disc anomaly | en | Synonym | Active | Case insensitive | SNOMED CT core |
4696048019 | A rare genetic eye disease with characteristics of congenital profound excavation of the optic nerve head with diminished visual field, in the absence of elevated intraocular pressure. Many patients lack a well-formed retinal artery and have multiple radial cilioretinal arteries instead. The condition is mostly bilateral, may worsen progressively, and is often complicated by serous macular detachment with profound visual loss. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set