Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3320913014 | Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3320914015 | Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | en | Synonym | Active | Case insensitive | SNOMED CT core |
3320915019 | A very rare mitochondrial respiratory chain deficiency described in fewer than 10 infants, primarily of middle Eastern descent, with clinical characteristics of transient but life-threatening liver failure with elevated liver enzymes, jaundice, vomiting, coagulopathy, hyperbilirubinemia, and lactic acidemia. | en | Definition | Active | Case sensitive | SNOMED CT core |
3320916018 | A very rare mitochondrial respiratory chain deficiency described in fewer than 10 infants, primarily of middle Eastern descent, with clinical characteristics of transient but life-threatening liver failure with elevated liver enzymes, jaundice, vomiting, coagulopathy, hyperbilirubinaemia, and lactic acidaemia. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | Finding site | Liver structure | true | Inferred relationship | Some | 1 | |
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | Clinical course | Acute | true | Inferred relationship | Some | 2 | |
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | Occurrence | Infancy | true | Inferred relationship | Some | 1 | |
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | Due to | Mitochondrial respiratory chain complexes disorder | true | Inferred relationship | Some | 3 | |
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | Is a | Acute digestive system disorder | true | Inferred relationship | Some | ||
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | Is a | Acute hepatic failure | true | Inferred relationship | Some | ||
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | Is a | Digestive system hereditary disorder | true | Inferred relationship | Some | ||
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | Occurrence | Infancy | false | Inferred relationship | Some | 2 | |
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | Clinical course | Acute | false | Inferred relationship | Some | 2 | |
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | Finding site | Liver structure | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set