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:0050735 | X-linked monogenic disease | A monogenic disease that has_material_basis_in mutations in genes on the X chromosome. |
329 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050735 | DOID:0050437 |
| is_a | DOID:0050735 | DOID:0050445 |
| is_a | DOID:0050735 | DOID:0050476 |
| is_a | DOID:0050735 | DOID:0050554 |
| is_a | DOID:0050735 | DOID:0050566 |
| is_a | DOID:0050735 | DOID:0050630 |
| is_a | DOID:0050735 | DOID:0050631 |
| is_a | DOID:0050735 | DOID:0050647 |
| is_a | DOID:0050735 | DOID:0050679 |
| is_a | DOID:0050735 | DOID:0050681 |
| is_a | DOID:0050735 | DOID:0050699 |
| is_a | DOID:0050177 | DOID:0050735 |
| is_a | DOID:630 | DOID:0050735 |
| is_a | DOID:4 | DOID:0050735 |
| is_a | DOID:0050735 | DOID:0050760 |
| is_a | DOID:0050735 | DOID:0050764 |
| is_a | DOID:0050735 | DOID:0050776 |
| is_a | DOID:0050735 | DOID:0050781 |
| is_a | DOID:0050735 | DOID:0050879 |
| is_a | DOID:0050735 | DOID:0050953 |
| is_a | DOID:0050735 | DOID:0060013 |
| is_a | DOID:0050735 | DOID:0060022 |
| is_a | DOID:0050735 | DOID:0060063 |
| is_a | DOID:0050735 | DOID:0060161 |
| is_a | DOID:0050735 | DOID:0060179 |
| is_a | DOID:0050735 | DOID:0060246 |
| is_a | DOID:0050735 | DOID:0060248 |
| is_a | DOID:0050735 | DOID:0060292 |
| is_a | DOID:0050735 | DOID:0060305 |
| is_a | DOID:0050735 | DOID:0060309 |
