8 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:0014667 | disease of metabolism | A disease that involving errors in metabolic processes of building or degradation of molecules. |
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
| DOID:0080015 | physical disorder | A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment. |
| DOID:655 | inherited metabolic disorder | A disease of metabolism that is characterized by enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to inherited enzyme abnormality. |
| DOID:0050718 | vitamin metabolic disorder | An inherited metabolic disorder resulting from a deficiency in vitamin or vitamin cofactor transport or metabolism. |
| DOID:0050731 | vitamin B12 deficiency | A vitamin metabolic disorder that results from low blood levels of vitamin B12. |
| DOID:0050734 | congenital intrinsic factor deficiency | A vitamin B12 deficiency that is characterized by megaloblastic anemia due to the absence of gastric intrinsic factor which results in abnormal vitamin B12 absorption. |
7 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050731 | DOID:0050734 |
| is_a | DOID:0080015 | DOID:0050734 |
| is_a | DOID:655 | DOID:0050734 |
| is_a | DOID:0014667 | DOID:0050734 |
| is_a | DOID:4 | DOID:0050734 |
| is_a | DOID:630 | DOID:0050734 |
| is_a | DOID:0050718 | DOID:0050734 |
