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 |
| 2995113011 | Der(22) syndrome due to 3:1 meiotic disjunction events | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2995222019 | Supernumerary der(22)t(11;22) syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2995585015 | Supernumerary derivative 22 chromosome syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 2995681016 | Emanuel syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 2995820019 | Supernumerary der(22)t(11;22) syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 2995830011 | Supernumerary der(22) syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Supernumerary der(22)t(11;22) syndrome | Is a | Congenital disorder due to abnormality of chromosome number OR structure | true | Inferred relationship | Existential restriction modifier | ||
| Supernumerary der(22)t(11;22) syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Supernumerary der(22)t(11;22) syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Supernumerary der(22)t(11;22) syndrome | Finding site | Chromosome structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR