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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 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