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 |
3323635016 | Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3323636015 | Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3323637012 | Grange syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3323638019 | Grange occlusive arterial syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome | Is a | Connective tissue hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome | Is a | Hereditary dysplasia of blood vessel | true | Inferred relationship | Existential restriction modifier | ||
Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome | Finding site | Connective tissue structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome | Finding site | Blood vessel structure | true | Inferred relationship | Existential restriction modifier | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets