1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111421 | familial apolipoprotein A5 deficiency | A familial chylomicronemia syndrome characterized by hyperchylomicronemia, elevated levels of very low density lipoprotein, and decreased LDL and HDL levels after fasting that has_material_basis_in heterozygous mutation in the APOA5 gene on chromosome 11q23.3. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0014667 | disease of metabolism | A disease that involving errors in metabolic processes of building or degradation of molecules. |
