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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

Condition name Status OMIM number Documents
Myoclonic Epilepsy and Ragged Red Fibres (MERRF) approved 545000
Myoclonic Epilepsy of Unverricht-Lundborg Disease (ULD-EPM1) approved 254800
Myoclonus Dystonia (DYT11) approved 159900
Myopathy, Myofibrillar 1 approved 601419
Myopathy, Myofibrillar 10 approved 619040
Myopathy, Myofibrillar 2 approved 608810
Myopathy, Myofibrillar 3 approved 609200
Myopathy, Myofibrillar 4 approved 609452
Myopathy, Myofibrillar 5 approved 609524
Myopathy, Myofibrillar 6 approved 612954
Myopathy, Myofibrillar 7 approved 617114
Myopathy, Myofibrillar 8 approved 617258
Myopathy, Myofibrillar 9 with early respiratory failure approved 603689
Myopathy, Myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related approved 613869
Myopathy, spheroid body, (due to mutations in the same gene as myopathy, myofibrillar 3 and with similar phenotype) approved 182920
Myotonia Congenita, Autosomal Dominant approved 160800
Myotonia Congenita, Autosomal Recessive approved 255700
Myotonic Dystrophy approved 160900
Myotonic Dystrophy type 2 approved 602668
Myotubular myopathy approved 310400, 300219