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 |
2968210013 | Heritable pulmonary arterial hypertension | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
2968226014 | Heritable pulmonary arterial hypertension (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Heritable pulmonary arterial hypertension | Is a | Pulmonary hypertensive arterial disease | true | Inferred relationship | Existential restriction modifier | ||
Heritable pulmonary arterial hypertension | Finding site | Pulmonary artery structure | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial primary pulmonary hypertension | Is a | True | Heritable pulmonary arterial hypertension | Inferred relationship | Existential restriction modifier | |
Sporadic primary pulmonary hypertension | Is a | True | Heritable pulmonary arterial hypertension | Inferred relationship | Existential restriction modifier | |
Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation | Is a | True | Heritable pulmonary arterial hypertension | Inferred relationship | Existential restriction modifier | |
Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation | Is a | True | Heritable pulmonary arterial hypertension | Inferred relationship | Existential restriction modifier | |
Braddock syndrome | Is a | True | Heritable pulmonary arterial hypertension | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets