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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
Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma (DCWHK) approved 605676
Cardiomyopathy, Dilated, with Woolly Hair, Keratoderma, and Tooth Agenesis (DCWHKTA) approved 615821
Cardiomyopathy, Familial Hypertrophic, 1 (CMH1) approved 192600
Cardiomyopathy, Familial Hypertrophic, 10 (CMH10) approved 608758
Cardiomyopathy, Familial Hypertrophic, 11 (CMH11) approved 612098
Cardiomyopathy, Familial Hypertrophic, 12 (CMH12) approved 612124
Cardiomyopathy, Familial Hypertrophic, 13 (CMH13) approved 613243
Cardiomyopathy, Familial Hypertrophic, 2 (CMH2) approved 115195
Cardiomyopathy, Familial Hypertrophic, 26 (CMH26) - to see minutes search for condition Arrhythmogenic Right Ventricular Cardiomyopathy 15 (ARVC15) approved 617047
Cardiomyopathy, Familial Hypertrophic, 27 (CMH27) approved 618052
Cardiomyopathy, Familial Hypertrophic, 28 (CMH28) approved 619402
Cardiomyopathy, Familial Hypertrophic, 3 (CMH3) approved 115196
Cardiomyopathy, Familial Hypertrophic, 4 (CMH4) approved 115197
Cardiomyopathy, Familial Hypertrophic, 6 (CMH6) approved 600858
Cardiomyopathy, Familial Hypertrophic, 7 (CMH7) approved 613690
Cardiomyopathy, Familial Hypertrophic, 8 (CMH8) approved 608751
Cardiomyopathy, Familial Restrictive, 5 (RCM5) - to see minutes search for condition Arrhythmogenic Right Ventricular Cardiomyopathy 15 (ARVC15) approved 617047
Carney Complex, Type 1 (CNC1) approved 160980
Carnitine Acylcarnitine Translocase Deficiency (CACT) approved 212138
Carpenter Syndrome 1 (CRPT1) approved 201000