CTAGE9
Description
The CTAGE9 (CTAGE family member 9) is a protein-coding gene located on chromosome 6.
CTAGE9 is also known as -.
Associated Diseases
- hypertriglyceridemia 2
- cholesterol-ester transfer protein deficiency
- hyperlipidemia due to hepatic triglyceride lipase deficiency
- homozygous familial hypercholesterolemia
- pancreatic triacylglycerol lipase deficiency
- thyroid hormone metabolism, abnormal, 2
- hypoalphalipoproteinemia, primary, 1
- sitosterolemia
- hypercholesterolemia, autosomal dominant, 3
- familial apolipoprotein C-II deficiency
- hypercholesterolemia, autosomal dominant, type B
- glycogen storage disease VI
- chylomicron retention disease
- familial hypobetalipoproteinemia 1
