PGT-M conditions
This table shows all PGT-M conditions currently approved and awaiting consideration by the HFEA.
Please note that we are updating this database, and some approved conditions may not be displayed. If you are unsure if a condition has been approved or not, please contact pgtm@hfea.gov.uk.
Download full approved condition list.
| Condition name | Status | OMIM number | Documents |
|---|---|---|---|
| Fanconi Anaemia, Complementation Group S | approved | 617883 | |
| Fanconi Anaemia, Complementation Group T | approved | 616435 | |
| Feingold syndrome 1 (FGLDS1) | approved | 164280 | |
| Fetal Akinesia Deformation Sequence (Pena-Shokeir syndrome type 1) | approved | 208150 | |
| Fibrodysplasia Ossificans Progressiva (FOP) | approved | 135100 | |
| Focal Dermal Hypoplasia (FDH) | approved | 305600 | |
| Focal Segmental Glomerulosclerosis 7 (FSGS7) | approved | 616002 | |
| Focal Segmental Glomerulosclerosis Type 1 | approved | 603278 | |
| Focal Segmental Glomerulosclerosis Type 2 | approved | 603965 | |
| Focal Segmental Glomerulosclerosis Type 5 | approved | 613237 | |
| Focal Segmental Glomerulosclerosis Type 6 | approved | 614131 | |
| Focal Segmental Glomerulosclerosis Type 8 | approved | 615032 | |
| Focal Segmental Glomerulosclerosis Type 9 | approved | 616220 | |
| Fontaine Progeroid Syndrome (FPS) | approved | 612289 | |
| Fragile X Syndrome (FRAX) | approved | 300624 | |
| Fragile XE syndrome (FRAXE) | approved | 309548 | |
| Fraser Syndrome | approved | 219000 | |
| Fraser syndrome-2 (FRASRS2) | awaiting approval | #617666 | |
| Friedreich Ataxia 1 (FRDA) | approved | 229300 | |
| Frontometaphyseal Dysplasia | approved | 305620 | |