4 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. |
| 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. |
3713 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050739 | DOID:0050156 |
| is_a | DOID:0050739 | DOID:0050331 |
| is_a | DOID:0050739 | DOID:0050335 |
| is_a | DOID:0050739 | DOID:0050424 |
| is_a | DOID:0050739 | DOID:0050427 |
| is_a | DOID:0050739 | DOID:0050429 |
| is_a | DOID:0050739 | DOID:0050430 |
| is_a | DOID:0050739 | DOID:0050434 |
| is_a | DOID:0050739 | DOID:0050436 |
| is_a | DOID:0050739 | DOID:0050438 |
| is_a | DOID:0050739 | DOID:0050439 |
| is_a | DOID:0050739 | DOID:0050441 |
| is_a | DOID:0050739 | DOID:0050449 |
| is_a | DOID:0050739 | DOID:0050450 |
| is_a | DOID:0050739 | DOID:0050462 |
| is_a | DOID:0050739 | DOID:0050463 |
| is_a | DOID:0050739 | DOID:0050465 |
| is_a | DOID:0050739 | DOID:0050466 |
| is_a | DOID:0050739 | DOID:0050469 |
| is_a | DOID:0050739 | DOID:0050470 |
| is_a | DOID:0050739 | DOID:0050471 |
| is_a | DOID:0050739 | DOID:0050472 |
| is_a | DOID:0050739 | DOID:0050473 |
| is_a | DOID:0050739 | DOID:0050474 |
| is_a | DOID:0050739 | DOID:0050475 |
| is_a | DOID:0050739 | DOID:0050524 |
| is_a | DOID:0050739 | DOID:0050528 |
| is_a | DOID:0050739 | DOID:0050529 |
| is_a | DOID:0050739 | DOID:0050530 |
| is_a | DOID:0050739 | DOID:0050540 |
