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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

Download full approved condition list.

Condition name Status OMIM number Documents
Cone Rod Dystrophy 18 (CORD18) approved 615374
Cone Rod Dystrophy 19 (CORD19) approved 615860
Cone Rod Dystrophy 2 (CORD2) approved 120970
Cone Rod Dystrophy 20 (CORD20) approved 615973
Cone Rod Dystrophy 21 (CORD 21) approved 616502
Cone Rod Dystrophy 3 (CORD3) approved 604232
Cone Rod Dystrophy 5 (CORD5) approved 600977
Cone Rod Dystrophy 6 (CORD6) approved 601777
Cone Rod Dystrophy 7 (CORD7) approved 603349
Cone Rod Dystrophy 9 (CORD9) approved 612775
Congenital Adrenal Hyperplasia (21 hydroxylase deficiency) approved 201910
Congenital Cataracts approved 601885
Congenital Contractual Arachnodactyly (Beals Syndrome) approved 121050
Congenital Deafness with inner ear agenesis, microtia and microdontia approved 610706
Congenital Disorder of Glycosylation type 1a (CDG1A) approved 212065
Congenital Disorder of Glycosylation type 1D (CDG1D) approved 601110
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