Primary Hypoalphalipoproteinemia 1
Disease ID: disease_node_16843
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| Dbxref | GARD:2872, MIM:604091, ORDO:425 |
|---|---|
| Subclassof | DOID_1387 |
| Data Source | DOID |
| Synonyms | familial HDL deficiency, familial hypoalphalipoproteinemia |
| Doid Label | primary hypoalphalipoproteinemia 1 |
| Doid Description | A hypolipoproteinemia that is characterized by low levels of high-density lipoprotein in the blood and that has_material_basis_in heterozygous mutation in the ABC1 gene on chromosome 9q31, which is also the site of mutations causing Tangier disease. |
| Disease Node Id | disease_node_16843 |
| Doid Id | DOID_0080957 |
| Label | Primary Hypoalphalipoproteinemia 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Hypolipoproteinemias(ID:disease_node_4190) (Disease)