Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1766599016 | Citrullinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1773235018 | Citrullinaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1774521013 | Citrullinemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4533531000146111 | citrullinemie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 14579811000146117 | citrullinemie (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Citrullinemia (disorder) | Is a | Enzymopathy | true | Inferred relationship | Some | ||
| Citrullinemia (disorder) | Is a | Aminoacidemia | true | Inferred relationship | Some | ||
| Citrullinemia (disorder) | Is a | Disorder of the urea cycle metabolism | true | Inferred relationship | Some | ||
| Citrullinemia (disorder) | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Citrullinemia (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Citrullinemia (disorder) | Is a | Hereditary disease | false | Inferred relationship | Some | ||
| Citrullinemia (disorder) | Is a | Hereditary metabolic disease | true | Inferred relationship | Some | ||
| Citrullinemia (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Citrullinemia (disorder) | Is a | Hereditary metabolic disease | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| laat optredende citrullinemie (aandoening) | Is a | False | Citrullinemia (disorder) | Inferred relationship | Some | |
| Citrullinemia, neonatal type | Is a | True | Citrullinemia (disorder) | Inferred relationship | Some | |
| Citrullinemia, subacute type | Is a | True | Citrullinemia (disorder) | Inferred relationship | Some | |
| Citrin deficiency (disorder) | Is a | True | Citrullinemia (disorder) | Inferred relationship | Some | |
| Citrullinemia type I (disorder) | Is a | True | Citrullinemia (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR