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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
Ectrodactyly, Ectodermal Dysplasia and Cleft Lip/Palate syndrome 3 (EEC3) approved 604292
Ectrodactyly, Ectodermal Dysplasia, Clefting Syndrome (EEC) approved 129900
Ehlers-Danlos periodontal type 1 (EDSPD1) approved 130080
Ehlers-Danlos periodontal type 2 (EDSPD2) approved 617174
Ehlers-Danlos Syndrome, Kyphoscoliotic, type 1 (EDSKSCL1) approved 225400
Ehlers-Danlos Syndrome, Kyphoscoliotic, type 2 (EDSKSCL2) approved 614557
Ehlers-Danlos Type IV approved 130050
Elastin (ELN)-related Supravalvular Aortic Stenosis approved 185500
Ellis-Van Crevald Syndrome approved 225500
Emery-Dreifuss Muscular Dystrophy (x-linked) (EDMD) (Male embryos only) approved 310300
Emery-Dreifuss muscular dystrophy 4 (EDMD4) approved 612998
Emery-Dreifuss muscular dystrophy 5 (EDMD5) approved 612999
Emery-Dreifuss muscular dystrophy 6 X-Linked (EDMD6) approved 300696
Emery-Dreifuss muscular dystrophy 7 (EDMD7) approved 614302
Emery-Dreifuss Muscular Dystrophy type 2 - for cases where there is proven evidence of mosaicism in the blood or as a result of a second affected child approved 181350
Emery-Dreifuss Muscular Dystrophy type 3 approved 616516
Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum (PEBAT) approved 617193
Epidermolysis Bullosa Simplex 1C, Localised (EBS1C) approved 131800
Epidermolysis Bullosa Simplex 2A, Generalized Severe; EBS2A awaiting approval #619555
Epidermolysis Bullosa Simplex 2C, Localised (EBS2C) approved 619594