Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2995041012 | Cerebral creatine deficiency syndrome 3 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2995201013 | Arginine:glycine amidinotransferase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2995208019 | L-arginine:glycine amidinotransferase deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 2995231019 | Creatine deficiency syndrome due to arginine:glycine amidinotransferase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2995424016 | Cerebral creatine deficiency syndrome 3 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Cerebral creatine deficiency syndrome 3 | Is a | Disorder of creatine synthesis | true | Inferred relationship | Existential restriction modifier | ||
| Cerebral creatine deficiency syndrome 3 | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Cerebral creatine deficiency syndrome 3 | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR