Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2968120014 | Heritable pulmonary arterial hypertension due to BMPR2 mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3008434016 | Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
3008454015 | Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation | Is a | Heritable pulmonary arterial hypertension | true | Inferred relationship | Existential restriction modifier | ||
Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation | Finding site | Pulmonary artery structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets