11 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:0050736 | autosomal dominant disease | An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease. |
| DOID:0050739 | autosomal genetic disease | A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes. |
| 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 | combined pituitary hormone deficiency | A hypopituitarism characterized by deficiency in growth hormone and at least one other pituitary hormone. |
| DOID:0061018 | combined or isolated pituitary hormone deficiency 8 | A combined pituitary hormone deficiency that has_material_basis_in heterozygous mutation in the ROBO1 gene on chromosome 3p12. |
10 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:9410 | DOID:0061018 |
| is_a | DOID:0050736 | DOID:0061018 |
| is_a | DOID:9406 | DOID:0061018 |
| is_a | DOID:0050177 | DOID:0061018 |
| is_a | DOID:53 | DOID:0061018 |
| is_a | DOID:0050739 | DOID:0061018 |
| is_a | DOID:7 | DOID:0061018 |
| is_a | DOID:630 | DOID:0061018 |
| is_a | DOID:4 | DOID:0061018 |
| is_a | DOID:28 | DOID:0061018 |
