Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 106778014 | Ethanolaminosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 106779018 | Ethanolamine kinase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 106780015 | Ethanolaminuria | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 803606017 | Ethanolaminosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Ethanolaminosis | Is a | Disorder of amino acid and organic acid metabolism | true | Inferred relationship | Some | ||
| Ethanolaminosis | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Ethanolaminosis | Is a | Enzymopathy | true | Inferred relationship | Some | ||
| Ethanolaminosis | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
| Ethanolaminosis | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Ethanolaminosis | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR