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 |
| 3425073016 | Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3425074010 | Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3425075011 | Transient neonatal multiple acyl-CoA dehydrogenase deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3425076012 | Transient neonatal glutaric acidemia type 2 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3425077015 | Transient neonatal glutaric acidaemia type 2 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3425078013 | Transient neonatal glutaric aciduria type 2 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3425079017 | Transient neonatal MAD (multiple acyl-coenzyme A dehydrogenase) deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency | Is a | Glutaric aciduria, type 2 | false | Inferred relationship | Existential restriction modifier | ||
| Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency | Is a | Neonatal disorder | false | Inferred relationship | Existential restriction modifier | ||
| Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency | Is a | Acute metabolic disorder | true | Inferred relationship | Existential restriction modifier | ||
| Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 3 | |
| Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency | Occurrence | Neonatal | true | Inferred relationship | Existential restriction modifier | 1 | |
| Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency | Clinical course | Transitory | true | Inferred relationship | Existential restriction modifier | 2 | |
| Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency | Is a | Neonatal metabolic disorder | true | Inferred relationship | Existential restriction modifier | ||
| Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency | Is a | Acyl-coenzyme A dehydrogenase deficiency | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR