Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-May 2025. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5457796010 | Coenzyme Q2, polyprenyltransferase gene related-coenzyme Q10 deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5457797018 | Coenzyme Q2, polyprenyltransferase gene related-coenzyme Q10 deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5457798011 | Primary coenzyme Q10 deficiency-1 | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5457799015 | COQ10D1- primary coenzyme Q10 deficiency-1 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5457800016 | COQ2-gene related coenzyme Q10 deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Coenzyme Q2, polyprenyltransferase gene related-coenzyme Q10 deficiency (disorder) | Is a | Coenzyme Q10 deficiency (disorder) | true | Inferred relationship | Some | ||
| Coenzyme Q2, polyprenyltransferase gene related-coenzyme Q10 deficiency (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR