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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
Deafness, Autosomal Recessive 6 (DFNB6) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 600971
Deafness, Autosomal Recessive 63 (DFNB63) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 611451
Deafness, Autosomal Recessive 67 (DFNB67) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 610265
Deafness, Autosomal Recessive 68 (DFNB68) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 610419
Deafness, Autosomal Recessive 7 (DFNB7) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 600974
Deafness, Autosomal Recessive 70, with or without Adult-Onset Neurodegeneration (DFNB70) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 614934
Deafness, Autosomal Recessive 74 (DFNB74) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 613718
Deafness, Autosomal Recessive 8/10 (DFNB8/10) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 601072
Deafness, Autosomal Recessive 84A (DFNB84A) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 613391
Deafness, Autosomal Recessive 89 (DFNB89) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 613916
Deafness, Autosomal Recessive 9 (DFNB9) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 601071
Deafness, Autosomal Recessive 93 (DFNB93) (due to publishing limitations, we can't provide a link to the relevant minutes - please contact HFEA.Licensing@HFEA.gov.uk if you would like to be sent a copy) approved 614899
Deafness, autosomal recessive, 29 (DFNB29) approved 614035
Deafness, Congenital, with Inner Ear Agenesis, Microtia and Microdontia approved 610706
Dehydrated Hereditary Stomatocytosis 1 with or without Pseudohyperkalemia and/or Perinatal Edema (DHS1) approved 194380
Dementia, Lewy Body (DLB) approved 127750
Dentatorubral-Pallidoluysian Atrophy (DRPLA) approved 125370
Dentinogenesis Imperfecta 1 (DGI1) approved 125490
Denys-Drash Syndrome (DDS) approved 194080
Desbuquois Dysplasia 1 (DBQD1) approved 251450