| Approved symbol | FBN2 |
|---|---|
| Approved name | fibrillin 2 |
| HGCN ID | HGNC:3604 |
| Previous symbols | CCA |
| Inheritance | |
| OMIM | 612570 |
| Chromosome | 5q23.3 |
| Panel(s) |
NGS Aortic and arterial dilatation/dissection NGS Congenital Heart Defects NGS Fetal akinesia deformation sequence FADS NGS Marfan syndrome and marfan-like disorders NGS Mendeliome NGS Skeletal Dysplasia |
