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 |
|---|---|---|---|
| Distal Hereditary Motor Neuropathy type IIB | approved | 608634 | |
| Distal Renal Tubular Acidosis with progressive nerve deafness | approved | 602722, 267300 | |
| Dominant Dystrophic Epidermolysis Bullosa | approved | 131750 | |
| Donnai-Barrow Syndrome | approved | 222448 | |
| Donohue Syndrome | approved | 246200 | |
| Dopamine Responsive Dystonia (DRD) | approved | 128230 | |
| Downs Syndrome | approved | 190685 | |
| Doyne honeycomb retinal dystrophy (DHRD) | approved | 126600 | |
| Dravet Syndrome (DEE6A) | approved | 607208 | |
| Duane-radial ray syndrome (Okihiro syndrome, acro-renal-ocular syndrome, SALL4-related Holt Oram syndrome) | approved | 607323 | |
| Dyskeratosis congenita (Male embryos only) | approved | 305000 | |
| Dyskeratosis Congenita types A2 and B4, due to TERT mutation | approved | 613989 | |
| Dystonia 1 Torsion Autosomal Dominant (DYT1) | approved | 128100 | |
| Dystonia 26, Myoclonic; DYT26 | awaiting approval | 616398 | |
| Early-onset progressive encephalopathy with brain atrophy and thin corpus callosum (PEBAT) | awaiting approval | 617193 | |
| Ectodermal dysplasia / skin fragility syndrome | approved | 604536 | |
| Ectrodactyly, Ectodermal Dysplasia and Cleft Lip/Palate syndrome 3 (EEC3) | approved | 604292 | |
| Ectrodactyly, Ectodermal Dysplasia, Clefting Syndrome (EEC) | approved | 129900 | |
| Ehlers-Danlos periodontal type 1 (EDSPD1) | approved | 130080 | |
| Ehlers-Danlos periodontal type 2 (EDSPD2) | approved | 617174 | |