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:0014667 | disease of metabolism | A disease that involving errors in metabolic processes of building or degradation of molecules. |
| DOID:18 | urinary system disease | A disease of anatomical entity that is located_in kidney, ureter, bladder and urethra. |
| DOID:557 | kidney disease | A urinary system disease that is located_in the kidney. |
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
| DOID:655 | inherited metabolic disorder | A disease of metabolism that is characterized by enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to inherited enzyme abnormality. |
| DOID:9252 | amino acid metabolic disorder | An inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids. |
| DOID:365 | bladder disease | A urinary system disease that is located_in the bladder. |
| DOID:1426 | ureteral disease | A urinary system disease that is located_in the ureter. |
| DOID:9266 | cystinuria | An amino acid metabolic disorder that involves the formation of cystine stones in the kidneys, ureter, and bladder. |
10 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:365 | DOID:9266 |
| is_a | DOID:557 | DOID:9266 |
| is_a | DOID:1426 | DOID:9266 |
| is_a | DOID:9252 | DOID:9266 |
| is_a | DOID:18 | DOID:9266 |
| is_a | DOID:7 | DOID:9266 |
| is_a | DOID:4 | DOID:9266 |
| is_a | DOID:655 | DOID:9266 |
| is_a | DOID:0014667 | DOID:9266 |
| is_a | DOID:630 | DOID:9266 |
