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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
Maturity-Onset Diabetes of the Young, Type 3 (MODY3) approved 600496
Meckel Syndrome, Type 1 (MKS1) approved 249000
Meckel Syndrome, Type 10 (MKS10) approved 614175
Meckel Syndrome, Type 11 (MKS11) approved 615397
Meckel Syndrome, Type 2 (MKS2) approved 603194
Meckel Syndrome, Type 3 (MKS3) approved 607361
Meckel Syndrome, Type 4 (MKS4) approved 611134
Meckel Syndrome, Type 5 (MKS5) approved 611561
Meckel Syndrome, Type 6 (MKS6) approved 612284
Meckel Syndrome, Type 7 (MKS7) approved 267010
Meckel Syndrome, Type 8 (MKS8) approved 613885
Meckel Syndrome, Type 9 (MKS9) approved 614209
MEDNIK Syndrome (MEDNIK) approved 609313
Medullary Cystic Kidney Disease 2 (MCKD2) (also known as Autosomal Dominant Tubulointerstitial Kidney Disease due to Uromodulin Mutations (ADTKD-UMOD) approved 603860
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 1 (MMIHS1) approved 249210
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 2 (MMIHS2) approved 619351
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 3 (MMIHS3) approved 619362
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 5 (MMIHS5) approved 619431
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 (MPPH1) approved 603387
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2 (MPPH2) approved 615937