PGT-M conditions
The page below lists all PGT-M conditions currently authorised and awaiting consideration by the HFEA.
When publishing genetic conditions on the authorised list, we aim to be as consistent as possible with the OMIM database. However, many conditions may have several different names and we would recommend searching the list using the OMIM number for the condition as this is less likely to change throughout time.
If a condition does not appear on the list, it does not necessarily mean the condition has specifically not been authorised, it may mean that we have never before received an application from a UK centre to perform PGT-M for this condition and it has therefore never been considered by the HFEA.
Please note that we are always processing new applications to add genetic conditions to the list from UK centres licensed to perform PGT-M. This may mean that some authorised conditions may not be displayed. If you are unsure if a condition has been authorised or not, or would like any further information please contact the PGTM team at pgtm@hfea.gov.uk.
Click here for a downloadable list: approved condition list. Please note that the website page below is updated more regularly and is therefore more accurate than the downloadable list.
| Condition name | Status | OMIM number | Documents |
|---|---|---|---|
| Neurofibromatosis, Type II (NF2) | approved | 101000 | |
| Neurologic, Endocrine and Pancreatic Disease, Multisystem, Infantile-Onset 2; IMNEPD2 | awaiting consideration | 619418 | |
| Neuronal Ceroid Lipofuscinosis Type 3 (Batten disease) (CLN3) | approved | 204200 | |
| Neuronopathy Distal Hereditary Motor, Type IX (HMN9) | approved | 617721 | |
| Neuronopathy, Distal Hereditary Motor, Type IIA (HMN2A) | approved | 158590 | |
| Neuronopathy, Distal Hereditary Motor, Type IIB (HMN2B) | approved | 608634 | |
| Neuronopathy, Distal Hereditary Motor, Type IIC (HMN2C) | approved | 613376 | |
| Neuronopathy, Distal Hereditary Motor, Type IID (HMN2D) | approved | 615575 | |
| Neuronopathy, Distal Hereditary Motor, Type VA (HMN5A) | approved | 600794 | |
| Neuronopathy, Distal Hereditary Motor, Type VB (HMN5B) | approved | 614751 | |
| Neuronopathy, Distal Hereditary Motor, Type VC (HMN5C) | approved | 619112 | |
| Neuronopathy, Distal Hereditary Motor, Type VIIA (HMN7A) | approved | 158580 | |
| Neuronopathy, Distal Hereditary Motor, Type VIIB (HMN7B) | approved | 607641 | |
| Neuronopathy, distal hereditary motor, type VIII (HMN8) | approved | 600175 | |
| Neuropathy, Ataxia, and Retinitis Pigmentosa (NARP Syndrome) | approved | 551500 | |
| Neuropathy, Congenital Hypomyelinating 1, Autosomal Recessive (CHN1) (also known as Charcot Marie-Tooth Disease, Type 4E (CMT4E)) | approved | 605253 | |
| Neuropathy, Congenital Hypomyelinating, 2, Autosomal Recessive (CHN2) | approved | 618184 | |
| Neuropathy, Congenital Hypomyelinating, 3, Autosomal Recessive (CHN3) | approved | 618186 | |
| Neuropathy, Hereditary Motor and Sensory, Russe Type (HMSNR) (also known as Charcot-Marie-Tooth Disease, Type 4G (CMT4G)) | approved | 605285 | |
| Neuropathy, Hereditary Sensory and Autonomic, Type IA (HSAN1A) | approved | 162400 | |
