| Anzahl | |
|---|---|
| Indication | |
| Hereditary breast and/or ovarian cancer syndrome (HGNC 1101) | 5 |
| Myotonic dystrophy type 1 (HGNC 2933) | 5 |
| Huntington’s disease (HGNC 4851) | 3 |
| Loeys-Dietz syndrome (HGNC 11772, 11773 or 11768) | 3 |
| Lynch syndrome (HGNC 7325, 7127 oder 7329) | 3 |
| Marfan syndrome (HGNC 3603) | 3 |
| Osteogenesis imperfecta type 1 (HGNC 2197 or 2198) | 3 |
PGT-M: Preimplantation genetic testing for monogenic disorders.
Source: FIVNAT/SFSO