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PGT-M conditions

This table shows all PGT-M 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 pgtm@hfea.gov.uk.

Download full approved condition list.

Condition name Status OMIM number Documents
Myasthenic syndrome, congenital, 20 approved 617143
Myasthenic syndrome, congenital, 21 approved 617239
Myasthenic syndrome, congenital, 22 approved 616224
Myasthenic syndrome, congenital, 24 approved 618198
Myasthenic syndrome, congenital, 25 approved 618323
Myasthenic syndrome, congenital, 2A, Slow-channel approved 616313
Myasthenic syndrome, congenital, 3B, Fast-channel approved 616322
Myasthenic syndrome, congenital, 4A, Slow-channel approved 605809
Myasthenic syndrome, congenital, 4B, Fast-channel approved 616324
Myasthenic syndrome, congenital, 4C approved 608931
Myasthenic syndrome, congenital, 6 approved 254210
Myasthenic syndrome, congenital, 7 approved 616040
Myasthenic syndrome, congenital, 8 approved 615120
Myasthenic syndrome, congenital, 9 approved 616325
Myoclonic Epilepsy and Ragged Red Fibres (MERRF) approved 545000
Myoclonic Epilepsy of Unverricht-Lundborg Disease (ULD-EPM1) approved 254800
Myoclonus Dystonia (DYT11) approved 159900
Myofibromatosis, Infantile, 1 (IMF1) approved 228550
Myopathy, Congenital, with Fiber-Type Disproportion (CFTD) approved 255310
Myopathy, Myofibrillar 1 approved 601419