Skip to main content

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
Congenital hereditary cataract, type 17 (CTRCT17) approved 611544
Congenital hereditary cataract, type 18 (CTRCT18) approved 610019
Congenital hereditary cataract, type 19 (CTRCT19) approved 615277
Congenital hereditary cataract, type 21 (CTRCT21) approved 610202
Congenital hereditary cataract, type 22 (CTRCT22) approved 609741
Congenital hereditary cataract, type 23 (CTRCT23) approved 610425
Congenital hereditary cataract, type 30 (CTRCT30) approved 116300
Congenital hereditary cataract, type 33 (CTRCT33) approved 611391
Congenital hereditary cataract, type 34 (CTRCT34) approved 612968
Congenital hereditary cataract, type 38 (CTRCT38) approved 614691
Congenital hereditary cataract, type 39 (CTRCT39) approved 615188
Congenital hereditary cataract, type 40 (CTRCT40) approved 302200
Congenital hereditary cataract, type 44 (CTRCT44) approved 616509
Congenital hereditary cataract, type 6 (CTRCT6) approved 116600
Congenital hereditary cataract, type 9 (CTRCT9) approved 604219
Congenital hypomyelinating neuropathy 1 approved 605253
Congenital hypomyelinating neuropathy 2 approved 618184
Congenital hypomyelinating neuropathy 3 (CHN3) approved 618186
Congenital Mitochondrial Encephalomyopathy approved 500002
Congenital stationary night blindness Type 1A (CSNB1A) approved 310500