Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3435711013 | Coenzyme Q10 deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 3435712018 | Coenzyme Q10 deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Coenzyme Q10 deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Coenzyme Q10 deficiency | Is a | Specific enzyme deficiency | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | True | Coenzyme Q10 deficiency | Inferred relationship | Some | |
| Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome | Is a | True | Coenzyme Q10 deficiency | Inferred relationship | Some | |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Due to | False | Coenzyme Q10 deficiency | Inferred relationship | Some | 4 |
| Deafness, encephaloneuropathy, obesity, valvulopathy syndrome | Due to | True | Coenzyme Q10 deficiency | Inferred relationship | Some | 5 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR