| Number | |
|---|---|
| Indication | |
| Cystic fibrosis (HGNC 1884) | 19 |
| Huntington’s disease (HGNC 4851) | 14 |
| Myotonic dystrophy type 1 (HGNC 2933) | 11 |
| Fragile X syndrome (HGNC 3775) | 11 |
| Family predisposition to breast cancer (HGNC 1100) | 6 |
PGT-M: Preimplantation genetic testing for monogenic disorders.
Source: FIVNAT/SFSO