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 pgd@hfea.gov.uk.
| 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 | |