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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
Cutis Laxa, autosomal recessive, type IIA (ARCL2A) approved 219200
Cutis Laxa, autosomal recessive, type IIB; ARCL2B approved 612940
Cutis Laxa, autosomal recessive, type IIC (ARCL2C), approved 617402
Cutis Laxa, autosomal recessive, type IID (ARCL2D) approved 617403
Cutis Laxa, autosomal recessive, type IIIA (ARCL3A) approved 219150
Cutis Laxa, autosomal recessive, type IIIB (ARCL3B) approved 614438
Cystic Fibrosis (CF) approved 219700
Czech Dysplasia, metatarsal type also known as Progressive pseudorheumatoid dysplasia with hypoplastic toes approved 609162
Danon Disease approved 300257
D-bifunctional protein deficiency approved 261515
Deafness, Autosomal Recessive 29; DFNB29 awaiting approval 614035
Deafness, autosomal recessive, 29 (DFNB29) approved 614035
Dehydrated hereditary stomatocytosis approved 194380
Dentatorubral-Pallidoluysian Atrophy (DRPLA) approved 125370
Denys-Drash Syndrome (DDS) approved 194080
Desbuquois Dysplasia 1 (DBQD1) approved 251450
Developmental and Epileptic Encephalopathy (DEE3) approved 609304
Developmental and Epileptic Encephalopathy 12 (DEE12) approved 613722
Developmental and Epileptic Encephalopathy 15 (DEE15) approved 615006
Developmental and Epileptic Encephalopathy 16 (DEE16) approved 615338