hyperalphalipoproteinemia 1

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Summary

Literature (0)

DOID:0111369 - hyperalphalipoproteinemia 1

Disease Ontology Definition: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 CETP gene on chromosome 16q13.

Synonyms: HALP1

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cetp

MIM:

MIM:143470 - HYPERALPHALIPOPROTEINEMIA 1; HALP1

MIM:143470 - HYPERALPHALIPOPROTEINEMIA 1; HALP1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), cholesterol-ester transfer protein deficiency (is_a)