• Source: Hypoalphalipoproteinemia

Hypoalphalipoproteinemia is a high-density lipoprotein deficiency, inherited in an autosomal dominant manner.
It can be associated with LDL receptor.
Associated regions and genes include:

Niacin is sometimes prescribed to raise HDL levels.




See also


CER-001




References






External links

Kata Kunci Pencarian:

• Hypoalphalipoproteinemia
• Tangier disease
• Hypolipoproteinemia
• List of genetic disorders
• List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders
• CER-001
• Apolipoprotein AI
• List of OMIM disorder codes