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