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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
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 Mitochondrial Encephalomyopathy approved 500002
Congenital stationary night blindness Type 1A (CSNB1A) approved 310500
Conradi-Hunermann-Happle Syndrome approved 302960
Constitutional MisMatch Repair Deficiency (CMMRD) awaiting approval 276300
Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis, approved 602066
Cowden syndrome (CS)/PTEN Hamartoma Tumour Syndrome (PHTS) approved 601728, 158350, 153480, 605309
Craniofrontonasal syndrome (CFNS) approved 304110
Crigler-Najjar Syndrome Type 1 (CN1) approved 218800