Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1231857010 | Leber hereditary optic neuropathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
1231858017 | LHON - Leber hereditary optic neuropathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
1231859013 | LHON - Leber's hereditary optic neuropathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
2839596015 | Leber optic atrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
797361019 | Leber's optic atrophy (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
97397016 | Leber's optic atrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Leber plus disease | Is a | True | Leber's optic atrophy | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set