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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
Lipodystrophy, Familial Partial, Type 2 (FPLD2) approved 151660
Lipodystrophy, Familial Partial, Type 3 (FPLD3) approved 162000
Lipodystrophy, Familial Partial, Type 4 (FPLD4) approved 613877
Lipodystrophy, Familial Partial, Type 6 (FPLD6) approved 615980
Lissencephaly 2 (LIS2) approved 257320
Lissencephaly 3 (LIS3) approved 611603
Lissencephaly 4 (LIS4) approved 614019
Lissencephaly 5 (LIS5) approved 615191
Lissencephaly 6 with Microcephaly (LIS6) approved 616212
Lissencephaly 8 (LIS8) approved 617255
Lissencephaly, X-Linked, 1 (LISX1) approved 300067
Lissencephaly, X-Linked, 2; LISX2 and Hydranencephaly with Abnormal Genitalia approved 300215
Loeys-Dietz Syndrome 1 (LDS1) approved 609192
Loeys-Dietz Syndrome 2 (LDS2) approved 610168
Loeys-Dietz Syndrome 3 (LDS3) approved 613795
Loeys-Dietz Syndrome 4 (LDS4) approved 614816
Long Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD) approved 609016
Long QT Syndrome 1 (LQT1) approved 192500
Long QT Syndrome 2 (LQT2) approved 613688
Long QT Syndrome 3 (LQT3) approved 603830