Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2003. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 315119018 | Osteopsathyrosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 590869014 | Osteopsathyrosis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Osteopsathyrosis | Is a | Osteogenesis imperfecta | false | Inferred relationship | Existential restriction modifier | ||
| Osteopsathyrosis | Finding site | Skeletal system structure | false | Inferred relationship | Existential restriction modifier | 1 | |
| Osteopsathyrosis | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Osteopsathyrosis | Finding site | Connective tissue | false | Inferred relationship | Existential restriction modifier | ||
| Osteopsathyrosis | Finding site | Bone structure | false | Inferred relationship | Existential restriction modifier | ||
| Osteopsathyrosis | Associated morphology | Dysplasia | false | Inferred relationship | Existential restriction modifier | 1 | |
| Osteopsathyrosis | Finding site | Connective tissue structure | false | Inferred relationship | Existential restriction modifier | ||
| Osteopsathyrosis | Associated morphology | Congenital dysplasia | false | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR