Hyperlipoproteinemia Type Iii
Disease ID: disease_node_4109
Connections displayed (default: 10).
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| Dbxref | MESH:D006952, MIM:617347, NCI:C34710, SNOMEDCT_US_2023_03_01:42569002, UMLS_CUI:C0020479 |
|---|---|
| Subclassof | DOID_1168 |
| Data Source | DOID, MESH |
| Synonyms | Remnant hyperlipidemia, carbohydrate induced hyperlipemia, familial hypercholesterolaemia with hyperlipaemia, familial type 3 hyperlipoproteinemia |
| Mesh Id | D006952 |
| Mesh Label | Hyperlipoproteinemia Type III |
| Mesh Subclassof | D008052, D006951 |
| Doid Label | hyperlipoproteinemia type III |
| Doid Description | A familial hyperlipidemia that has_material_basis_in by homozygous, compound heterozygous, or heterozygous mutation in the APOE gene on chromosome 19q13. |
| Disease Node Id | disease_node_4109 |
| Doid Id | DOID_3145 |
| Label | Hyperlipoproteinemia Type Iii |
- Outgoing r'ship
SUBCLASS_OFto/from Hyperlipidemias(ID:disease_node_4103) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hyperlipoproteinemias(ID:disease_node_4108) (Disease)