Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3317474016 | 8p11.2 deletion syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3317475015 | 8p11.2 deletion syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3317476019 | Monosomy 8p11.2 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| 8p11.2 deletion syndrome | Is a | 8p partial monosomy syndrome | true | Inferred relationship | Existential restriction modifier | ||
| 8p11.2 deletion syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
| 8p11.2 deletion syndrome | Finding site | Chromosome pair 8 | true | Inferred relationship | Existential restriction modifier | 2 | |
| 8p11.2 deletion syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 3 | |
| 8p11.2 deletion syndrome | Finding site | Chromosome pair 8 | true | Inferred relationship | Existential restriction modifier | 3 | |
| 8p11.2 deletion syndrome | Associated morphology | Deletion of short arm | true | Inferred relationship | Existential restriction modifier | 2 | |
| 8p11.2 deletion syndrome | Associated morphology | Partial monosomy | true | Inferred relationship | Existential restriction modifier | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR