Status: current, Primitive. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2981569019 | Inherited aminoaciduria | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2981621014 | Inherited aminoaciduria (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inherited aminoaciduria | Is a | Hereditary metabolic disease | true | Inferred relationship | Some | ||
| Inherited aminoaciduria | Is a | Hereditary disease | false | Inferred relationship | Some | ||
| Inherited aminoaciduria | Is a | Aminoaciduria | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Chorea due to inherited aminoaciduria | Due to | True | Inherited aminoaciduria | Inferred relationship | Some | 2 |
| Benign neonatal hyperaminoaciduria | Is a | False | Inherited aminoaciduria | Inferred relationship | Some | |
| Dicarboxylic aminoaciduria syndrome | Is a | True | Inherited aminoaciduria | Inferred relationship | Some | |
| Camptodactyly taurinuria syndrome | Is a | True | Inherited aminoaciduria | Inferred relationship | Some | |
| Deficiency of aminoacylase 1 | Is a | True | Inherited aminoaciduria | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR