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DO Term : primary hypoalphalipoproteinemia 1 [DOID:0080957] Disease Ontology

Namespace  disease_ontology Obsolete  false
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.
  • synonyms:
  • familial HDL deficiency,
  • OMIM:604091,
  • ORDO:425,
  • familial hypoalphalipoproteinemia,
  • 604091,
  • GARD:2872
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents