Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 493531016 | Hypermethioninaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 71937014 | Hypermethioninemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 780099018 | Hypermethioninemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypermethioninaemia | Is a | Disorder of sulfur-bearing amino acid metabolism | true | Inferred relationship | Some | ||
| Hypermethioninaemia | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Hypermethioninaemia | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Neonatal hypermethioninaemia | Is a | True | Hypermethioninaemia | Inferred relationship | Some | |
| Hepatic methionine adenosyltransferase deficiency | Is a | True | Hypermethioninaemia | Inferred relationship | Some | |
| Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | Is a | True | Hypermethioninaemia | Inferred relationship | Some | |
| Hypermethioninaemia due to deficiency of glycine N-methyltransferase | Is a | True | Hypermethioninaemia | Inferred relationship | Some | |
| Hypermethioninaemia encephalopathy due to deficiency of adenosine kinase | Is a | True | Hypermethioninaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR