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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.

Condition name Status OMIM number Documents
Charcot-Marie-Tooth disease, axonal, type 2P (CMT2P) approved 614436
Charcot-Marie-Tooth Disease, Type 4A (CMT4A) approved 214400
Charcot-Marie-Tooth Disease, Type 4B1 (CMT4B1) approved 601382
Charcot-Marie-Tooth Disease, Type 4B2 (CMT4B2) approved 604563
Charcot-Marie-Tooth Disease, Type 4B3 (CMT4B3) approved 615284
Charcot-Marie-Tooth Disease, Type 4C (CMT4C) approved 601596
Charcot-Marie-Tooth Disease, Type 4D (CMT4D) approved 601455
Charcot-Marie-Tooth Disease, Type 4F (CMT4F) approved 614895
Charcot-Marie-Tooth Disease, Type 4G (CMT4G) approved 605285
Charcot-Marie-Tooth Disease, Type 4H (CMT4H) approved 609311
Charcot-Marie-Tooth Disease, Type 4K (CMT4K) approved 616684
CHARGE Syndrome approved 214800
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