Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3643486017 | Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3643487014 | Hypermethioninemia encephalopathy due to deficiency of adenosine kinase | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3643488016 | Hypermethioninaemia encephalopathy due to deficiency of adenosine kinase | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3643489012 | Hypermethioninemia encephalopathy due to ADK (adenosine kinase) deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3643490015 | Hypermethioninaemia encephalopathy due to ADK (adenosine kinase) deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase | Due to | Deficiency of adenosine kinase | true | Inferred relationship | Existential restriction modifier | 2 | |
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase | Is a | Hypermethioninemia | true | Inferred relationship | Existential restriction modifier | ||
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase | Is a | Metabolic encephalopathy | true | Inferred relationship | Existential restriction modifier | ||
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier | ||
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase | Finding site | Brain structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hypermethioninemia encephalopathy due to deficiency of adenosine kinase | Is a | Central nervous system complication | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR