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 |
| 3638176013 | COXPD21 - combined oxidative phosphorylation defect type 21 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3638177016 | Combined oxidative phosphorylation defect type 21 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3638178014 | Combined oxidative phosphorylation defect type 21 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Combined oxidative phosphorylation defect type 21 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Combined oxidative phosphorylation defect type 21 | Is a | Mitochondrial cytopathy | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR