Skip to main content
HFEA wins prestigious award for data dashboard.Our award-winning dashboard gives users the opportunity to explore HFEA data and find statistics on their own areas of interest. Find out more here.

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
Fraser Syndrome 3 (FRASRS3) approved 617667
Friedreich Ataxia 1 (FRDA) approved 229300
Frontometaphyseal Dysplasia approved 305620
Frontotemporal Dementia approved 600274
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 approved 615911
Frontotemporal dementia and/or Amyotrophic lateral sclerosis 3 approved 616437
Frontotemporal dementia and/or Amyotrophic lateral sclerosis 4 approved 616439
Fucosidosis approved 230000
Galactosaemia approved 230400
Galactosialidosis (early infantile and adult / juvenile types) (GSL) approved 256540
Gangliosidosis (GM1) approved 230500
Gastrointestinal defects and immunodeficiency syndrome (GIDID) approved 243150
Gaucher Disease Type II approved 230900
Gaucher Disease Type III approved 231000
Generalized epilepsy with febrile seizures plus, type 1 (GEFSP1) approved 604233
Generalized epilepsy with febrile seizures plus, type 2 (GEFSP2) approved 604403
Generalized epilepsy with febrile seizures plus, type 3 (GEFSP3) approved 607681
Generalized epilepsy with febrile seizures plus, type 5, susceptibility to, (GEFSP5) approved 613060
Geroderma Osteodysplasticum approved 231070
Gerstmann-Straussler-Scheinker syndrome approved 137440