Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2995211018 | Childhood myocerebrohepatopathy spectrum (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2995462018 | Childhood myocerebrohepatopathy spectrum | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Childhood myocerebrohepatopathy spectrum | Is a | Mitochondrial cytopathy | true | Inferred relationship | Some | ||
| Childhood myocerebrohepatopathy spectrum | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Childhood myocerebrohepatopathy spectrum | Occurrence | Childhood | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR