Skip to main content
The HFEA has launched its new Media Centre where you can find the latest news and information from us. Access it 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
Congenital hereditary cataract, type 21 (CTRCT21) approved 610202
Congenital hereditary cataract, type 22 (CTRCT22) approved 609741
Congenital hereditary cataract, type 23 (CTRCT23) approved 610425
Congenital hereditary cataract, type 30 (CTRCT30) approved 116300
Congenital hereditary cataract, type 33 (CTRCT33) approved 611391
Congenital hereditary cataract, type 34 (CTRCT34) approved 612968
Congenital hereditary cataract, type 38 (CTRCT38) approved 614691
Congenital hereditary cataract, type 39 (CTRCT39) approved 615188
Congenital hereditary cataract, type 40 (CTRCT40) approved 302200
Congenital hereditary cataract, type 44 (CTRCT44) approved 616509
Congenital hereditary cataract, type 6 (CTRCT6) approved 116600
Congenital hereditary cataract, type 9 (CTRCT9) approved 604219
Congenital hypomyelinating neuropathy 1 approved 605253
Congenital hypomyelinating neuropathy 2 approved 618184
Congenital hypomyelinating neuropathy 3 (CHN3) approved 618186
Congenital Mitochondrial Encephalomyopathy approved 500002
Congenital stationary night blindness Type 1A (CSNB1A) approved 310500
Conradi-Hunermann-Happle Syndrome approved 302960
Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis, approved 602066
Corpus Callosum, Agenesis of, with Abnormal Genitalia approved 300004