Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2968210013 | Heritable pulmonary arterial hypertension | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2968226014 | Heritable pulmonary arterial hypertension (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
950721000172117 | FPAH - familial pulmonary arterial hypertension | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
959011000172118 | hypertension artérielle pulmonaire héréditaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3419191001000112 | Pulmonale arterielle Hypertonie, hereditäre | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Heritable pulmonary arterial hypertension | Is a | Pulmonary hypertensive arterial disease (disorder) | true | Inferred relationship | Some | ||
Heritable pulmonary arterial hypertension | Finding site | Pulmonary artery structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial primary pulmonary hypertension | Is a | True | Heritable pulmonary arterial hypertension | Inferred relationship | Some | |
Sporadic primary pulmonary hypertension | Is a | True | Heritable pulmonary arterial hypertension | Inferred relationship | Some | |
Heritable pulmonary arterial hypertension due to BMPR2 mutation | Is a | True | Heritable pulmonary arterial hypertension | Inferred relationship | Some | |
Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation | Is a | True | Heritable pulmonary arterial hypertension | Inferred relationship | Some | |
Braddock syndrome is a rare malformation syndrome with multiple congenital abnormalities, described in 2 siblings, that is characterized by VACTERL -like association in combination with pulmonary hypertension, laryngeal webs, blue sclerae, abnormal ears, persistent growth deficiency and normal intellect. | Is a | True | Heritable pulmonary arterial hypertension | Inferred relationship | Some |
This concept is not in any reference sets