Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3640229011 | Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3640230018 | COXPD12 - combined oxidative phosphorylation defect type 12 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3640231019 | Combined oxidative phosphorylation defect type 12 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3640232014 | Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome | Is a | Leukoencephalopathy | true | Inferred relationship | Existential restriction modifier | ||
| Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier | ||
| Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome | Is a | Mitochondrial cytopathy | true | Inferred relationship | Existential restriction modifier | ||
| Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome | Finding site | Cerebral white matter structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR