Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 49474011 | Leigh's disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 49475012 | Infantile necrotizing encephalomyelopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 49476013 | Subacute necrotizing encephalopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 49477016 | Subacute necrotizing encephalomyelopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 484329016 | Subacute necrotising encephalomyelopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 484330014 | Subacute necrotising encephalopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 484331013 | Infantile necrotising encephalomyelopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 760478017 | Leigh's disease (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| 1216300016 | SNEM - Subacute necrotising encephalomyelopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 1217799019 | SNEM - Subacute necrotizing encephalomyelopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 1226375014 | Leigh syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 2842378010 | Leigh disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 2951694017 | Leighs disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Maternally inherited Leigh syndrome | Is a | True | Leigh's disease | Inferred relationship | Existential restriction modifier | |
| Congenital lactic acidosis Saguenay-Lac-Saint-Jean type | Is a | True | Leigh's disease | Inferred relationship | Existential restriction modifier | |
| Leigh syndrome with nephrotic syndrome | Is a | True | Leigh's disease | Inferred relationship | Existential restriction modifier | |
| Dystonia due to Leigh syndrome | Due to | True | Leigh's disease | Inferred relationship | Existential restriction modifier | 3 |
| Leigh syndrome due to cytochrome C oxidase deficiency | Is a | True | Leigh's disease | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets