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:3952 | adrenal cortex disease | An adrenal gland disease that is located_in the adrenal cortex. |
| DOID:0060280 | primary pigmented nodular adrenocortical disease | An adrenal cortex disease characterized by small to normal sized adrenal glands containing multiple small cortical pigmented nodules. |
| DOID:0070548 | primary pigmented nodular adrenocortical disease 3 | A primary pigmented nodular adrenocortical disease that has_material_basis_in heterozygous mutation in the PDE8B gene on chromosome 5q13.3. |
6 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0060280 | DOID:0070548 |
| is_a | DOID:3952 | DOID:0070548 |
| is_a | DOID:4 | DOID:0070548 |
| is_a | DOID:7 | DOID:0070548 |
| is_a | DOID:9553 | DOID:0070548 |
| is_a | DOID:28 | DOID:0070548 |
