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:77 | gastrointestinal system disease | A disease of anatomical entity that is located_in the gastrointestinal tract. |
| 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:5295 | intestinal disease | A gastrointestinal system disease that is located_in the intestine. |
| DOID:0050589 | inflammatory bowel disease | An intestinal disease characterized by inflammation located in all parts of digestive tract. |
| DOID:0110886 | inflammatory bowel disease 9 | An inflammatory bowel disease that has_material_basis_in variation in the chromosome region 3p26. |
7 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050589 | DOID:0110886 |
| is_a | DOID:0050177 | DOID:0110886 |
| is_a | DOID:7 | DOID:0110886 |
| is_a | DOID:630 | DOID:0110886 |
| is_a | DOID:4 | DOID:0110886 |
| is_a | DOID:5295 | DOID:0110886 |
| is_a | DOID:77 | DOID:0110886 |
