Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1234911010 | Alpha, alpha-trehalase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 139627012 | Trehalose intolerance | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 201127011 | Trehalase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4636710019 | Trehalase deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Trehalase deficiency | Is a | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
| Trehalase deficiency | Is a | Specific enzyme deficiency | true | Inferred relationship | Some | ||
| Trehalase deficiency | Is a | Disorder of carbohydrate transport | true | Inferred relationship | Some | ||
| Trehalase deficiency | Is a | Enzymopathy | false | Inferred relationship | Some | ||
| Trehalase deficiency | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
| Trehalase deficiency | Is a | Disorder of carbohydrate absorption | true | Inferred relationship | Some | ||
| Trehalase deficiency | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
| Trehalase deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Trehalase deficiency | 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