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 |
| 3313302016 | Progressive osseous heteroplasia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3313303014 | Progressive osseous heteroplasia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3315787012 | Familial ectopic ossification | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Progressive osseous heteroplasia | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Progressive osseous heteroplasia | Is a | Disorder: ectopic bone tissue, congenital | true | Inferred relationship | Existential restriction modifier | ||
| Progressive osseous heteroplasia | Is a | Muscular ossification | true | Inferred relationship | Existential restriction modifier | ||
| Progressive osseous heteroplasia | Associated morphology | Osseous metaplasia | true | Inferred relationship | Existential restriction modifier | 1 | |
| Progressive osseous heteroplasia | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Progressive osseous heteroplasia | Finding site | Skeletal and/or smooth muscle 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