Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3704188015 | Monosomy 9p | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3704189011 | 9p deletion syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3704190019 | Monosomy 9p (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3704191015 | Alfi syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Monosomy 9p | Associated morphology | Partial monosomy | true | Inferred relationship | Existential restriction modifier | 2 | |
| Monosomy 9p | Finding site | Chromosome pair 9 | true | Inferred relationship | Existential restriction modifier | 1 | |
| Monosomy 9p | Finding site | Chromosome pair 9 | true | Inferred relationship | Existential restriction modifier | 2 | |
| Monosomy 9p | Associated morphology | Deletion of short arm | true | Inferred relationship | Existential restriction modifier | 1 | |
| Monosomy 9p | Is a | Deletion of part of chromosome 9 | true | Inferred relationship | Existential restriction modifier | ||
| Monosomy 9p | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Monosomy 9p | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR