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: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: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:447 | renal tubular transport disease | |
DOID:445 | Bartter disease |
13 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:445 | DOID:0110142 |
is_a | DOID:445 | DOID:0110143 |
is_a | DOID:445 | DOID:0110144 |
is_a | DOID:445 | DOID:0110145 |
is_a | DOID:445 | DOID:0110146 |
is_a | DOID:445 | DOID:0110147 |
is_a | DOID:0050177 | DOID:445 |
is_a | DOID:447 | DOID:445 |
is_a | DOID:7 | DOID:445 |
is_a | DOID:557 | DOID:445 |
is_a | DOID:4 | DOID:445 |
is_a | DOID:630 | DOID:445 |
is_a | DOID:18 | DOID:445 |