5 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:225 | syndrome | A disease characterized by a group of signs and symptoms that occur together and characterize a particular abnormality. |
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:10983 | Alport syndrome | A syndrome disease that is characterized by glomerulonephritis, endstage kidney disease, and hearing loss. |
7 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:10983 | DOID:0110032 |
is_a | DOID:10983 | DOID:0110033 |
is_a | DOID:10983 | DOID:0110034 |
is_a | DOID:0050177 | DOID:10983 |
is_a | DOID:225 | DOID:10983 |
is_a | DOID:630 | DOID:10983 |
is_a | DOID:4 | DOID:10983 |