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PGD conditions

This table shows all PGD 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

Condition name Status OMIM number Documents
CFHR5 Deficiency approved 614809
Charcot Marie Tooth Disease (x-linked) approved 302800
Charcot Marie Tooth Disease Type 2 approved 609260
Charcot Marie Tooth Disease, demyelinating type 1A (CMT1A) approved 118220
Charcot Marie Tooth type 1B (CM1B) approved 118200
Charcot Marie Tooth type 1C (CM1C) approved 601098
Charcot Marie Tooth type 1D (CM1D) approved 607678
Charcot Marie Tooth type 1E (CM1E) approved 118300
Charcot-Marie-Tooth disease, axonal, type 2P (CMT2P) approved OMIM #614436
CHARGE Syndrome approved 214800
Chondrodysplasia Punctata approved 302950
Choroideraemia approved 303100
Christianson syndrome approved 300243
Chromosomal rearrangements (various) approved
Citrullinaemia type 1 approved 215700
Claes-Jensen type X-linked recessive intellectual disability awaiting approval 300534
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