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 | |