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PGT-M conditions

This table shows all PGT-M conditions currently approved and awaiting consideration by the HFEA.

Please note that we are updating this database, and some approved conditions may not be displayed. If you are unsure if a condition has been approved or not, please contact pgtm@hfea.gov.uk.

Download full approved condition list.

Condition name Status OMIM number Documents
Cholestasis, progressive familial intrahepatic 2 (PFIC2) approved 601847
Cholestasis, progressive familial intrahepatic 3 (PFIC3) approved 602347
Cholestasis, progressive familial intrahepatic 4 (PFIC4) approved 615878
Cholestasis, progressive familial intrahepatic 5 (PFIC5) approved 617049
Cholestasis, progressive familial intrahepatic 8 (PFIC8) approved 619662
Cholestasis, progressive familial intrahepatic 9 (PFIC9) approved 619849
Cholestasis, progressive familial intrahepatic with or without hearing loss 7 (PFIC7) approved 619658
Cholestasis, progressive Familial Intrahepatic10 (PFIC10) approved 619868
Chondrodysplasia Punctata approved 302950
Choroideraemia approved 303100
Christianson syndrome approved 300243
Chromosomal rearrangements (various) approved
Chudley-McCullough Syndrome (CMCS) approved 604213
Citrullinaemia type 1 approved 215700
Classical Ehlers Danlos Syndrome approved 130000, 130010
Cleidocranial Dysplasia (CCD) approved 119600
Cockayne Syndrome type A and B approved 216400, 133540
Coenzyme Q10 Deficiency, Primary, 1 approved 607426
Coffin-Lowry Syndrome (CLS) approved 303600
Cohen Syndrome (COH1) approved 216550