7 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
| DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
| DOID:28 | endocrine system disease | A disease of anatomical entity that is located_in endocrine glands which secretes a type of hormone directly into the bloodstream to regulate the body. |
| DOID:9553 | adrenal gland disease | An endocrine system disease that is located_in the adrenal gland. |
| DOID:446 | primary hyperaldosteronism | An adrenal gland hyperfunction disease that results in the overproduction of aldosterone by the adrenal glands. |
| DOID:3947 | adrenal gland hyperfunction | |
| DOID:14080 | glucocorticoid-remediable aldosteronism | A primary hyperaldosteronism characterized by variably expressed and severe hypertension, hyperaldosteronism and abnormal adrenal steroid production which improve with exogenous glucocorticoid administration that has_material_basis_in a chimeric gene formed of the CYP11B2 and CYP11B1 genes on chromosome 8q24.3. |
6 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:446 | DOID:14080 |
| is_a | DOID:3947 | DOID:14080 |
| is_a | DOID:7 | DOID:14080 |
| is_a | DOID:9553 | DOID:14080 |
| is_a | DOID:28 | DOID:14080 |
| is_a | DOID:4 | DOID:14080 |
