Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
158184017 | Congenital anomaly of optic nerve | en | Synonym | Active | Case insensitive | SNOMED CT core |
839670015 | Congenital anomaly of optic nerve (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Severe X-linked intellectual disability Gustavson type | Is a | True | Congenital anomaly of optic nerve | Inferred relationship | Some | |
Combined immunodeficiency with faciooculoskeletal anomalies syndrome | Is a | True | Congenital anomaly of optic nerve | Inferred relationship | Some | |
CAMOS syndrome | Is a | True | Congenital anomaly of optic nerve | Inferred relationship | Some | |
Hypoplasia of the optic nerve | Is a | True | Congenital anomaly of optic nerve | Inferred relationship | Some | |
Congenital anomaly of optic disc | Is a | True | Congenital anomaly of optic nerve | Inferred relationship | Some | |
Oculocerebral dysplasia syndrome | Is a | False | Congenital anomaly of optic nerve | Inferred relationship | Some | |
Aplasia of optic nerve | Is a | True | Congenital anomaly of optic nerve | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set