Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
99817019 | Aldosterone deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
798999019 | Aldosterone deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1232041011 | Hypoaldosteronism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4587011000241110 | déficit en aldostérone | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Aldosterone deficiency | Is a | Adrenal cortical hypofunction | false | Inferred relationship | Some | ||
Aldosterone deficiency | Is a | Aldosterone disorder | true | Inferred relationship | Some | ||
Aldosterone deficiency | Interprets | Nutritional deficiency (finding) | false | Inferred relationship | Some | ||
Aldosterone deficiency | Finding site | Adrenal cortex structure | true | Inferred relationship | Some | 1 | |
Aldosterone deficiency | Finding site | Entire endocrine gonad (body structure) | false | Inferred relationship | Some | ||
Aldosterone deficiency | Is a | Adrenal cortical hypofunction (disorder) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hyporeninemic hypoaldosteronism | Is a | True | Aldosterone deficiency | Inferred relationship | Some | |
Hyperreninemic hypoaldosteronism | Is a | True | Aldosterone deficiency | Inferred relationship | Some | |
Corticosterone 18-monooxygenase deficiency | Is a | True | Aldosterone deficiency | Inferred relationship | Some | |
A rare inherited defect of the final step of aldosterone biosynthesis (conversion of deoxycorticosterone to aldosterone). It is due to mutations of the /CYP11B2/ (aldosterone synthase) gene and usually presents in infancy as a life-threatening electrolyte imbalance. | Is a | True | Aldosterone deficiency | Inferred relationship | Some |
This concept is not in any reference sets