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PGT-M conditions

The page below lists all PGT-M conditions currently authorised and awaiting consideration by the HFEA.

When publishing genetic conditions on the authorised list, we aim to be as consistent as possible with the OMIM database. However, many conditions may have several different names and we would recommend searching the list using the OMIM number for the condition as this is less likely to change throughout time.

If a condition does not appear on the list, it does not necessarily mean the condition has specifically not been authorised, it may mean that we have never before received an application from a UK centre to perform PGT-M for this condition and it has therefore never been considered by the HFEA.

Please note that we are always processing new applications to add genetic conditions to the list from UK centres licensed to perform PGT-M. This may mean that some authorised conditions may not be displayed. If you are unsure if a condition has been authorised or not, or would like any further information please contact the PGTM team at pgtm@hfea.gov.uk.

Click here for a downloadable list: approved condition list. Please note that the website page below is updated more regularly and is therefore more accurate than the downloadable list.

Condition name Status OMIM number Documents
Combined Oxidative Phosphorylation Deficiency 28 (COXPD28) approved 616794
Combined Oxidative Phosphorylation Deficiency 29 (COXPD29) approved 616811
Combined Oxidative Phosphorylation Deficiency 3 (COXPD3) approved 610505
Combined Oxidative Phosphorylation Deficiency 30 (COXPD30) approved 616974
Combined Oxidative Phosphorylation Deficiency 31 (COXPD31) approved 617228
Combined Oxidative Phosphorylation Deficiency 32 (COXPD32) approved 617664
Combined Oxidative Phosphorylation Deficiency 33 (COXPD33) approved 617713
Combined Oxidative Phosphorylation Deficiency 34 (COXPD34) approved 617872
Combined Oxidative Phosphorylation Deficiency 35 (COXPD35) approved 617873
Combined Oxidative Phosphorylation Deficiency 36 (COXPD36) approved 617950
Combined Oxidative Phosphorylation Deficiency 4 (COXPD4) approved 610678
Combined Oxidative Phosphorylation Deficiency 5 (COXPD5) approved 611719
Combined Oxidative Phosphorylation Deficiency 7 (COXPD7) approved 613559
Combined Oxidative Phosphorylation Deficiency 8 (COXPD8) approved 614096
Combined Oxidative Phosphorylation Deficiency 9 (COXPD9) approved 614582
Cone Rod Dystrophy 10 (CORD10) approved 610283
Cone Rod Dystrophy 11 (CORD11) approved 610381
Cone Rod Dystrophy 12 (CORD12) approved 612657
Cone Rod Dystrophy 13 (CORD13) approved 608194
Cone Rod Dystrophy 14 (CORD14) approved 602093