FNDC7
Description
The FNDC7 (fibronectin type III domain containing 7) is a protein-coding gene located on chromosome 1.
FNDC7 is also known as -.
Associated Diseases
- hypertriglyceridemia 2
- hypoalphalipoproteinemia, primary, 2, intermediate
- cholesterol-ester transfer protein deficiency
- plasma fibronectin deficiency
- thyroid hormone metabolism, abnormal, 2
- sitosterolemia
- homozygous familial hypercholesterolemia
- hypercholesterolemia, autosomal dominant, 3
- hyperlipoproteinemia type V
- hyperlipidemia due to hepatic triglyceride lipase deficiency
- hypercholesterolemia, autosomal dominant, type B
- familial apolipoprotein C-II deficiency
- pancreatic triacylglycerol lipase deficiency
- congenital enteropathy due to enteropeptidase deficiency
- congenital diarrhea 7 with exudative enteropathy
- glycogen storage disease VI
- TMEM199-CDG
- chylomicron retention disease
