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:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
DOID:0060388 | chromosomal deletion syndrome | A chromosomal disease that has_material_basis_in partial deletion of chromosomes. |
DOID:0080014 | chromosomal disease | A genetic disease that has_material_basis_in extra, missing, or re-arranged chromosomes. |
70 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:0060388 | DOID:0050460 |
is_a | DOID:0060388 | DOID:0060352 |
is_a | DOID:0080014 | DOID:0060388 |
is_a | DOID:4 | DOID:0060388 |
is_a | DOID:630 | DOID:0060388 |
is_a | DOID:0060388 | DOID:0060389 |
is_a | DOID:0060388 | DOID:0060390 |
is_a | DOID:0060388 | DOID:0060391 |
is_a | DOID:0060388 | DOID:0060392 |
is_a | DOID:0060388 | DOID:0060393 |
is_a | DOID:0060388 | DOID:0060394 |
is_a | DOID:0060388 | DOID:0060395 |
is_a | DOID:0060388 | DOID:0060396 |
is_a | DOID:0060388 | DOID:0060397 |
is_a | DOID:0060388 | DOID:0060398 |
is_a | DOID:0060388 | DOID:0060399 |
is_a | DOID:0060388 | DOID:0060400 |
is_a | DOID:0060388 | DOID:0060401 |
is_a | DOID:0060388 | DOID:0060402 |
is_a | DOID:0060388 | DOID:0060403 |
is_a | DOID:0060388 | DOID:0060404 |
is_a | DOID:0060388 | DOID:0060405 |
is_a | DOID:0060388 | DOID:0060406 |
is_a | DOID:0060388 | DOID:0060407 |
is_a | DOID:0060388 | DOID:0060408 |
is_a | DOID:0060388 | DOID:0060409 |
is_a | DOID:0060388 | DOID:0060410 |
is_a | DOID:0060388 | DOID:0060411 |
is_a | DOID:0060388 | DOID:0060412 |
is_a | DOID:0060388 | DOID:0060413 |