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 |
|---|---|---|---|
| Crouzon Syndrome | approved | 123500 | |
| Crouzon with acanthosis nigrans syndrome | approved | 612247 | |
| Currarino Syndrome | approved | 176450 | |
| Cutis Laxa, autosomal dominant 1 (ADCL1) | approved | 123700 | |
| Cutis Laxa, autosomal recessive, type IA (ARCL1A) | approved | 219100 | |
| Cutis Laxa, autosomal recessive, type IB (ARCL1B) | approved | 614437 | |
| Cutis Laxa, autosomal recessive, type IC (ARCL1C) | approved | 613177 | |
| 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 3; DFNB3 | awaiting approval | #600316 | |
| Deafness, autosomal recessive, 29 (DFNB29) | approved | 614035 | |
| Dehydrated hereditary stomatocytosis | approved | 194380 | |