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Disease Ontology Browser
primary hypoalphalipoproteinemia 1 (DOID:0080957)
Alliance: disease page
Synonyms: familial HDL deficiency; familial hypoalphalipoproteinemia
Alt IDs: OMIM:604091, ORDO:425
Definition: 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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory