Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3308295018 | Maternally inherited Leigh syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3308296017 | Maternally inherited Leigh syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3308297014 | Maternally inherited Leigh disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3308298016 | Maternally inherited infantile subacute necrotizing encephalopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3308299012 | Maternally inherited infantile subacute necrotising encephalopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3308300016 | A rare subtype of Leigh syndrome with clinical characteristics of encephalopathy, lactic acidosis, seizures, cardiomyopathy, respiratory disorders and developmental delay. Onset in infancy or early childhood resulting from maternally-inherited mutations in mitochondrial DNA. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Maternally inherited Leigh syndrome (disorder) | morphologie associée (attribut) | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
| Maternally inherited Leigh syndrome (disorder) | est un(e) (attribut) | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | true | Inferred relationship | Some | ||
| Maternally inherited Leigh syndrome (disorder) | survenue (attribut) | Infancy (qualifier value) | true | Inferred relationship | Some | 1 | |
| Maternally inherited Leigh syndrome (disorder) | est un(e) (attribut) | Leigh's disease | true | Inferred relationship | Some | ||
| Maternally inherited Leigh syndrome (disorder) | morphologie associée (attribut) | dégénérescence | false | Inferred relationship | Some | 1 | |
| Maternally inherited Leigh syndrome (disorder) | localisation d'une constatation (attribut) | structure de l'encéphale | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR