Hyperalphalipoproteinemia 1 (HALP1)

Alias:
Hyperalphalipoproteinemia
Cholesterol-Ester Transfer Protein Deficiency
Cholesteryl Ester Transfer Protein Deficiency
Cetp Deficiency
Halp1
Familial Hyperalphalipoproteinemia
Cept Deficiency
Cholesterol Ester Transfer Protein Deficiency
Familial Hyperalphalipoproteinemia Type I
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hyperalphalipoproteinemia 1, also known as hyperalphalipoproteinemia, is related to apolipoprotein c-iii deficiency and coronary stenosis. An important gene associated with Hyperalphalipoproteinemia 1 is CETP (Cholesteryl Ester Transfer Protein), and among its related pathways/superpathways are Metabolism and Transport of inorganic cations/anions and amino acids/oligopeptides. The drugs Adenosine and Pharmaceutical Solutions have been mentioned in the context of this disorder. Affiliated tissues include heart and adipocyte, and related phenotypes are hyperlipidemia and hypercholesterolemia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
Unknown
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13
109
36

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Mutations
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Related Drugs

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Status
Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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