Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 1766599016 | Citrullinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| 1773235018 | Citrullinaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 1774521013 | Citrullinemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 1786524014 | Argininosuccinate synthase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 1786525010 | ASS deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| 1786526011 | ASA synthase deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| 1786527019 | Argininosuccinase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 1786528012 | ASAS deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| 1786529016 | Arginosuccinate synthetase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Citrullinemia | Is a | Enzymopathy | true | Inferred relationship | Existential restriction modifier | ||
| Citrullinemia | Is a | Aminoacidemia | true | Inferred relationship | Existential restriction modifier | ||
| Citrullinemia | Is a | Disorder of the urea cycle metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Citrullinemia | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Citrullinemia | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Citrullinemia | Is a | Hereditary disease | false | Inferred relationship | Existential restriction modifier | ||
| Citrullinemia | Is a | Hereditary metabolic disease | true | Inferred relationship | Existential restriction modifier | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Citrullinemia, late-onset type | Is a | True | Citrullinemia | Inferred relationship | Existential restriction modifier | |
| Citrullinemia, neonatal type | Is a | True | Citrullinemia | Inferred relationship | Existential restriction modifier | |
| Citrullinemia, subacute type | Is a | True | Citrullinemia | Inferred relationship | Existential restriction modifier | |
| Citrin deficiency | Is a | True | Citrullinemia | Inferred relationship | Existential restriction modifier | |
| Citrullinemia type I | Is a | True | Citrullinemia | Inferred relationship | Existential restriction modifier | 
This concept is not in any reference sets