11 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: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:0050739 | autosomal genetic disease | A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes. |
| DOID:0050737 | autosomal recessive disease | An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop. |
| 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:0111418 | familial apolipoprotein C-II deficiency | A familial chylomicronemia syndrome characterized by onset in adolescence or adulthood of hypertriglyceridemia and fasting chylomicronemia that has_material_basis_in homozygous or compound heterozygous mutation in the APOC2 gene on chromosome 19q13.32. |
10 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050737 | DOID:0111418 |
| is_a | DOID:0111417 | DOID:0111418 |
| is_a | DOID:655 | DOID:0111418 |
| is_a | DOID:0050177 | DOID:0111418 |
| is_a | DOID:4 | DOID:0111418 |
| is_a | DOID:0014667 | DOID:0111418 |
| is_a | DOID:0050739 | DOID:0111418 |
| is_a | DOID:630 | DOID:0111418 |
| is_a | DOID:3146 | DOID:0111418 |
| is_a | DOID:1168 | DOID:0111418 |
