| 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 en gerelateerde aandoeningen NGS Marfan syndroom en andere marfanachtige beelden NGS Mendelioom NGS Osteogenesis imperfecta en gerelateerde aandoeningen |
