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: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:3146 | lipid metabolism disorder | An inherited metabolic disorder that involves the creation and degradation of lipids. |
| DOID:1168 | familial hyperlipidemia | |
| DOID:0111417 | familial chylomicronemia syndrome | A familial hyperlipidemia characterized by hypertriglyceridemia and fasting chylomicronemia. |
| DOID:0111419 | familial chylomicronemia due to inhibition of lipoprotein lipase activity | A familial chylomicronemia syndrome characterized by hypertriglyceridemia, chylomicronemia, very low levels of postheparin plasma lipolytic activity, presence in the circulation of a lipoprotein lipase inhibitor, and elevated adipose levels of lipoprotien lipase. |
7 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0111417 | DOID:0111419 |
| is_a | DOID:655 | DOID:0111419 |
| is_a | DOID:0014667 | DOID:0111419 |
| is_a | DOID:4 | DOID:0111419 |
| is_a | DOID:1168 | DOID:0111419 |
| is_a | DOID:630 | DOID:0111419 |
| is_a | DOID:3146 | DOID:0111419 |
