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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
Congenital Disorder of Glycosylation, Type 1m; CDG1M approved 610768
Congenital Disorder of Glycosylation, Type 1n; CDG1N approved 612015
Congenital Disorder of Glycosylation, Type 1p; CDG1P approved 613661
Congenital Disorder of Glycosylation, Type 1q; CDG1Q approved 612379
Congenital Disorder of Glycosylation, Type 1r; CDG1R approved 614507
Congenital Disorder of Glycosylation, Type 1t; CDG1T approved 614921
Congenital Disorder of Glycosylation, Type 1u; CDG1U approved 615042
Congenital Disorder of Glycosylation, Type 1w; CDG1W approved 615596
Congenital Disorder of Glycosylation, Type 1x; CDG1X approved 615597
Congenital Disorder of Glycosylation, Type 1y; CDG1Y approved 300934
Congenital Disorder of Glycosylation, Type Ik; CDG1K approved 608540
Congenital Dyserythropoietic Anaemia types 1a, 1b and 2 approved 224120, 615631, 224100
Congenital Fibrosis of the extraocular muscles (CFEOM1 and CFEOM3B) approved 135700
Congenital Heart Defects, Multiple Types 6 (CHTD6) (NB this relates to the autosomal recessive type of the condition only) approved 613854
Congenital Hemidysplasia with Ichthyosiform Erythrodema and Limb Defects (CHILD) syndrome approved 308050
Congenital hereditary cataract, type 10 (CTRCT10) approved 600881
Congenital hereditary cataract, type 11 (CTRCT11) approved 610623
Congenital hereditary cataract, type 12 (CTRCT12) approved 611597
Congenital hereditary cataract, type 15 (CTRCT15) approved 615274
Congenital hereditary cataract, type 16 (CTRCT16) approved 613763