Skip to main content

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
Muscular Dystrophy (Oculopharangeal)(OPMD) approved 164300
Muscular dystrophy, congenital, Davignon-Chauveau type approved 617066
Muscular dystrophy, congenital, due to Integrin alpha-7 deficiency approved 613204
Muscular Dystrophy, Congenital, LMNA-related, (MDCL) - for cases where there is proven evidence of mosaicism in the blood or as a result of a second affected child approved 613205
Muscular dystrophy, congenital, megaconial type approved 602541
Muscular dystrophy, congenital, with cataracts and intellectual disability approved 617404
Muscular dystrophy, Limb-Girdle (LGMD) Type 1B approved 159001
Muscular dystrophy, limb-girdle, autosomal recessive 17 approved 613723
Muscular dystrophy, limb-girdle, type 2C approved 253700
Muscular dystrophy, limb-girdle, type 2S approved 615356
Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B1 approved 613155
Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B14 approved 615351
Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2 approved 613156
Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B3 approved 613151
Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B6 approved 608840
Muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B5 approved 606612
Muscular dystrophy-dystroglycanopathy (limb-girdle), type C1 approved 609308
Muscular dystrophy-dystroglycanopathy (limb-girdle), type C5 approved 607155
Muscular dystrophy-dystroglycanopathy (limb-girdle), type C7 approved 616052
Muscular dystrophy-dystroglycanopathy, type A1 (Walker Warburg Syndrome) approved 236670