Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3994439013 | 11p15 duplication syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3994440010 | 11p15 duplication syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| 11p15 duplication syndrome | Is a | 11p partial trisomy syndrome | true | Inferred relationship | Existential restriction modifier | ||
| 11p15 duplication syndrome | Finding site | Chromosome pair 11 | true | Inferred relationship | Existential restriction modifier | 1 | |
| 11p15 duplication syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| 11p15 duplication syndrome | Associated morphology | Partial trisomy | true | Inferred relationship | Existential restriction modifier | 1 | |
| 11p15 duplication syndrome | Is a | Congenital malformation | true | Inferred relationship | Existential restriction modifier | ||
| 11p15 duplication syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR