CFC1B
Description
The CFC1B (cryptic, EGF-CFC family member 1B) is a protein-coding gene located on chromosome 2.
CFC1B is also known as -.
Associated Diseases
- visceral heterotaxy
- right atrial isomerism
- congenital heart defects, multiple types, 6
- heterotaxy, visceral, 5, autosomal
- tricuspid atresia
- heterotaxy, visceral, 9, autosomal, with male infertility
- Meacham syndrome
- ciliary dyskinesia, primary, 40
- atrial septal defect, ostium primum type
- ciliary dyskinesia, primary, 39
- ventricular septal defect 1
- congenital heart defects, multiple types, 7
- 22q11.2 deletion syndrome
- fallot complex-intellectual disability-growth delay syndrome
- conotruncal heart malformations
- deafness, congenital heart defects, and posterior embryotoxon
