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DO Term : apolipoprotein C-III deficiency [DOID:0111370] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A cholesterol-ester transfer protein deficiency characterized by elevated levels of alpha-lipoprotein in the blood that has_material_basis_in heterozygous mutation in the APOC3 gene on chromosome 11q23.3.
  • synonyms:
  • hyperalphalipoproteinemia 2,
  • OMIM:614028,
  • 614028,
  • MESH:C566270,
  • HALP2
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Disease

Diseases --> Human genes

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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