Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3663230012 | Pseudohyperaldosteronism type 2 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3663233014 | Early-onset hypertension with exacerbation in pregnancy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3663234015 | Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3663235019 | Hypertension due to gain-of-function mutation in mineralocorticoid receptor | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3663236018 | A rare genetic hypertension with characteristics of a familial severe hypertension with an onset before age 20 years, associated with suppressed plasma renin and low aldosterone levels in the presence of low or normal levels of the mineralocorticoid aldosterone, that is highly resistant to antihypertensive medication. During pregnancy, there is a marked exacerbation of hypertension, accompanied by low serum potassium levels and undetectable aldosterone levels, but without signs of preeclampsia, requiring early delivery. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5404714010 | A rare genetic cause of hypertension characterized by severe early-onset therapy-resistant hypertension due to a gain-of-function mutation in the mineralocorticoid receptor. The condition is associated with suppressed plasma renin activity and low serum aldosterone levels and is markedly exacerbated during pregnancy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5404715011 | A rare genetic cause of hypertension characterised by severe early-onset therapy-resistant hypertension due to a gain-of-function mutation in the mineralocorticoid receptor. The condition is associated with suppressed plasma renin activity and low serum aldosterone levels and is markedly exacerbated during pregnancy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) | Finding site | Systemic circulatory system structure | true | Inferred relationship | Some | 2 | |
| Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) | Is a | Secondary hypertension | true | Inferred relationship | Some | ||
| Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) | Interprets | Blood pressure | true | Inferred relationship | Some | 1 | |
| Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) | Has interpretation | Increased | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR