Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3440703015 | Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A synthase (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3440704014 | 3-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3440705010 | 3-hydroxy-3-methylglutaryl-CoA synthase deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3440706011 | Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A synthase | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3440707019 | HMG-coenzyme A synthase deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A synthase | Is a | Disorder of fatty acid metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A synthase | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A synthase | Is a | Specific enzyme deficiency | true | Inferred relationship | Existential restriction modifier | ||
| Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A synthase | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR