| Approved symbol | EMILIN1 |
|---|---|
| Approved name | elastin microfibril interfacer 1 |
| HGCN ID | HGNC:19880 |
| Previous symbols | |
| Inheritance | |
| OMIM | 130660 |
| Chromosome | 2p23.3 |
| Panel(s) |
NGS Cutis laxa and related disorders NGS Marfan syndrome and marfan-like disorders NGS Mendeliome NGS Osteogenesis imperfecta and related disorders |
