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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
Diarrhea 5, with Tufting Enteropathy, Congenital (DIAR5) approved 613217
Diarrhea 8, Secretory Sodium, Congenital (DIAR8) approved 616868
Diarrheoa 5 with tufting enteropathy congenital (DIAR5) approved 613217
Dihydrolipoamide Dehydrogenase Deficiency (DLDD) approved 246900
Distal Hereditary Motor Neuropathy type IIB approved 608634
Distal Renal Tubular Acidosis with progressive nerve deafness approved 602722, 267300
Dominant Dystrophic Epidermolysis Bullosa approved 131750
Donnai-Barrow Syndrome approved 222448
Donohue Syndrome approved 246200
Dopamine Responsive Dystonia (DRD) approved 128230
Downs Syndrome approved 190685
Doyne honeycomb retinal dystrophy (DHRD) approved 126600
Dravet Syndrome (DEE6A) approved 607208
Duane-radial ray syndrome (Okihiro syndrome, acro-renal-ocular syndrome, SALL4-related Holt Oram syndrome) approved 607323
Dyskeratosis congenita (Male embryos only) approved 305000
Dyskeratosis Congenita types A2 and B4, due to TERT mutation approved 613989
Dystonia 1 Torsion Autosomal Dominant (DYT1) approved 128100
Dystonia 12; DYT12 approved 128235
Dystonia 16; DYT16 approved 612067
Dystonia 2, Torsion, Autosomal Recessive; DYT2 approved 224500