3 Parents
Identifier | Name | Description |
---|---|---|
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: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. |
4107 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:0050177 | DOID:0050144 |
is_a | DOID:0050177 | DOID:0050156 |
is_a | DOID:630 | DOID:0050177 |
is_a | DOID:4 | DOID:0050177 |
is_a | DOID:0050177 | DOID:0050331 |
is_a | DOID:0050177 | DOID:0050335 |
is_a | DOID:0050177 | DOID:0050424 |
is_a | DOID:0050177 | DOID:0050427 |
is_a | DOID:0050177 | DOID:0050429 |
is_a | DOID:0050177 | DOID:0050430 |
is_a | DOID:0050177 | DOID:0050434 |
is_a | DOID:0050177 | DOID:0050436 |
is_a | DOID:0050177 | DOID:0050437 |
is_a | DOID:0050177 | DOID:0050438 |
is_a | DOID:0050177 | DOID:0050439 |
is_a | DOID:0050177 | DOID:0050441 |
is_a | DOID:0050177 | DOID:0050445 |
is_a | DOID:0050177 | DOID:0050449 |
is_a | DOID:0050177 | DOID:0050450 |
is_a | DOID:0050177 | DOID:0050451 |
is_a | DOID:0050177 | DOID:0050462 |
is_a | DOID:0050177 | DOID:0050463 |
is_a | DOID:0050177 | DOID:0050465 |
is_a | DOID:0050177 | DOID:0050466 |
is_a | DOID:0050177 | DOID:0050467 |
is_a | DOID:0050177 | DOID:0050469 |
is_a | DOID:0050177 | DOID:0050470 |
is_a | DOID:0050177 | DOID:0050471 |
is_a | DOID:0050177 | DOID:0050472 |
is_a | DOID:0050177 | DOID:0050473 |