8 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:0111622 | ACTH-independent macronodular adrenal hyperplasia | A primary hyperaldosteronism characterized by multiple bilateral adrenocortical nodules that cause a striking enlargement of the adrenal gland and production of an excess of cortisol. |
DOID:0111623 | ACTH-independent macronodular adrenal hyperplasia 1 | An ACTH-independent macronodular adrenal hyperplasia that has_material_basis_in somatic mutation in the GNAS gene on chromosome 20q13.32. |
7 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:0111622 | DOID:0111623 |
is_a | DOID:7 | DOID:0111623 |
is_a | DOID:9553 | DOID:0111623 |
is_a | DOID:28 | DOID:0111623 |
is_a | DOID:4 | DOID:0111623 |
is_a | DOID:3947 | DOID:0111623 |
is_a | DOID:446 | DOID:0111623 |