Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial hyperaldosteronism | Is a | Primary hyperaldosteronism (disorder) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Familial hyperaldosteronism | Finding site | Adrenal cortex structure | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Familial hyperaldosteronism | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Familial hyperaldosteronism | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Existential restriction modifier (core metadata concept) |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial hyperaldosteronism type 1 | Is a | True | Familial hyperaldosteronism | Inferred relationship | Existential restriction modifier (core metadata concept) | |
Familial hyperaldosteronism type 2 | Is a | True | Familial hyperaldosteronism | Inferred relationship | Existential restriction modifier (core metadata concept) | |
Familial hyperaldosteronism type 3 (disorder) | Is a | True | Familial hyperaldosteronism | Inferred relationship | Existential restriction modifier (core metadata concept) | |
A rare familial hyperaldosteronism characterized by elevated aldosterone levels and low plasma renin activity, early-onset hypertension, and hypokalemia. Developmental delay, learning disabilities, behavioral abnormalities, and attention deficit disorder are observed in some patients. | Is a | True | Familial hyperaldosteronism | Inferred relationship | Existential restriction modifier (core metadata concept) |
This concept is not in any reference sets