Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 71937014 | Hypermethioninemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 71938016 | Hypermethioninemia, NOS | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 493531016 | Hypermethioninaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 780099018 | Hypermethioninemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 936531000052115 | hypermetioninemi | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypermethioninemia | Is a | Disorder of sulphur-bearing amino acid metabolism | true | Inferred relationship | Some | ||
| Hypermethioninemia | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Hypermethioninemia | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Neonatal hypermethioninemia | Is a | True | Hypermethioninemia | Inferred relationship | Some | |
| Hepatic methionine adenosyltransferase deficiency | Is a | True | Hypermethioninemia | Inferred relationship | Some | |
| Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (disorder) | Is a | True | Hypermethioninemia | Inferred relationship | Some | |
| Hypermethioninemia due to deficiency of glycine N-methyltransferase | Is a | True | Hypermethioninemia | Inferred relationship | Some | |
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder) | Is a | True | Hypermethioninemia | Inferred relationship | Some |
This concept is not in any reference sets
FHIR