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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
Congenital Disorder of Glycosylation type 1D (CDG1D) approved 601110
Congenital Disorder of Glycosylation, Type 1b; CDG1B approved 602579
Congenital Disorder of Glycosylation, Type 1c; CDG1C approved 603147
Congenital Disorder of Glycosylation, Type 1cc; CDG1CC approved 301031
Congenital Disorder of Glycosylation, Type 1e; CDG1E approved 608799
Congenital Disorder of Glycosylation, Type 1f; CDG1F approved 609180
Congenital Disorder of Glycosylation, Type 1g; CDG1G, approved 607143
Congenital Disorder of Glycosylation, Type 1h; CDG1H approved 608104
Congenital Disorder of Glycosylation, Type 1i; G1I approved 607906
Congenital Disorder of Glycosylation, Type 1j; CDG1J approved 608093
Congenital Disorder of Glycosylation, Type 1l; CDG1L approved 608776
Congenital Disorder of Glycosylation, Type 1m; CDG1M approved 610768
Congenital Disorder of Glycosylation, Type 1n; CDG1N approved 612015
Congenital Disorder of Glycosylation, Type 1p; CDG1P approved 613661
Congenital Disorder of Glycosylation, Type 1q; CDG1Q approved 612379
Congenital Disorder of Glycosylation, Type 1r; CDG1R approved 614507
Congenital Disorder of Glycosylation, Type 1t; CDG1T approved 614921
Congenital Disorder of Glycosylation, Type 1u; CDG1U approved 615042
Congenital Disorder of Glycosylation, Type 1w; CDG1W approved 615596
Congenital Disorder of Glycosylation, Type 1x; CDG1X approved 615597