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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

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, 1A; CMD1A approved 115200
Cardiomyopathy, dilated, 1D; CMD1D approved 601494
Cardiomyopathy, dilated, 1DD (CMD1DD) approved 613172
Cardiomyopathy, dilated, 1P; CMD1P approved 609909
Cardiomyopathy, Dilated, 1PP (CMD1PP) approved 617047
Cardiomyopathy, dilated, 1S; CMD1S approved 613426
Cardiomyopathy, dilated, 1Y; CMD1Y approved 611878
Cardiomyopathy, Dilated, Type 1G (CMD1G) approved 604145
Cardiomyopathy, Dilated, Type 1HH (CMD1HH) approved 613881
Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma (DCWHK) approved 605676
Cardiomyopathy, Dilated, with Woolly Hair, Keratoderma, and Tooth Agenesis (DCWHKTA) approved 615821
Cardiomyopathy, dilated1MM/LVNC10 approved 615396
Cardiomyopathy, Familial Hypertrophic, 26 (CMH26) approved 617047
Cardiomyopathy, Familial Restrictive, 5 (RCM5) approved 617047
Carney Complex approved 160980
Carnitine Acylcarnitine Translocase Deficiency (CACT) approved 212138
Carpenter Syndrome 1 approved 201000
Carpenter Syndrome 2 approved 614976
Cartilage-Hair Hypoplasia approved 250250
Cartilage-hair hypoplasia spectrum approved 157660