10 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:0050177 | monogenic disease | A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive. |
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
| DOID:0050735 | X-linked monogenic disease | A monogenic disease that has_material_basis_in mutations in genes on the X chromosome. |
| DOID:9406 | hypopituitarism | A pituitary gland disease characterized by the decreased secretion of one or more of the eight hormones normally produced by the pituitary gland. |
| DOID:53 | pituitary gland disease | An endocrine system disease that is located_in the pituitary gland. |
| DOID:9410 | panhypopituitarism | A hypopituitarism characterized by deficiency in growth hormone and at least one other pituitary hormone. |
| DOID:0111779 | X-linked panhypopituitarism | A panhypopituitarism that has_material_basis_in duplications in the SOX3 gene on chromosome Xq27.1. |
9 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:9410 | DOID:0111779 |
| is_a | DOID:0050735 | DOID:0111779 |
| is_a | DOID:4 | DOID:0111779 |
| is_a | DOID:7 | DOID:0111779 |
| is_a | DOID:28 | DOID:0111779 |
| is_a | DOID:630 | DOID:0111779 |
| is_a | DOID:0050177 | DOID:0111779 |
| is_a | DOID:53 | DOID:0111779 |
| is_a | DOID:9406 | DOID:0111779 |
