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 |
| 3655792019 | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3655793012 | Hepatoencephalopathy due to COXPD1 (combined oxidative phosphorylation defect type 1) | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3655794018 | Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | Is a | Hepatic encephalopathy | true | Inferred relationship | Existential restriction modifier | ||
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier | ||
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | Is a | Metabolic and genetic disorder affecting the liver | true | Inferred relationship | Existential restriction modifier | ||
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | Is a | Digestive system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | Finding site | Brain structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | Finding site | Liver structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | Due to | Disorder of liver | true | Inferred relationship | Existential restriction modifier | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR