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 |
|---|---|---|---|
| Cone Rod Dystrophy 6, CORD6 | awaiting approval | 601777 | |
| Cone Rod Dystrophy 7 (CORD7) | approved | 603349 | |
| Cone Rod Dystrophy 9 (CORD9) | approved | 612775 | |
| Congenital Adrenal Hyperplasia (21 hydroxylase deficiency) | approved | 201910 | |
| Congenital Adrenal Insufficiency | awaiting approval | 613743 | |
| Congenital Cataracts | approved | 601885 | |
| Congenital Contractual Arachnodactyly (Beals Syndrome) | approved | 121050 | |
| Congenital Deafness with inner ear agenesis, microtia and microdontia | approved | 610706 | |
| Congenital Disorder of Glycosylation type 1a (CDG1A) | approved | 212065 | |
| Congenital Disorder of Glycosylation type 1D (CDG1D) | approved | 601110 | |
| Congenital Dyserythropoietic Anaemia types 1a, 1b and 2 | approved | 224120, 615631, 224100 | |
| Congenital Fibrosis of the extraocular muscles (CFEOM1 and CFEOM3B) | approved | 135700 | |
| Congenital hereditary cataract, type 10 (CTRCT10) | approved | 600881 | |
| Congenital hereditary cataract, type 11 (CTRCT11) | approved | 610623 | |
| Congenital hereditary cataract, type 12 (CTRCT12) | approved | 611597 | |
| Congenital hereditary cataract, type 15 (CTRCT15) | approved | 615274 | |
| Congenital hereditary cataract, type 16 (CTRCT16) | approved | 613763 | |
| Congenital hereditary cataract, type 17 (CTRCT17) | approved | 611544 | |
| Congenital hereditary cataract, type 18 (CTRCT18) | approved | 610019 | |
| Congenital hereditary cataract, type 19 (CTRCT19) | approved | 615277 | |