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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 I (NF1) approved 162200
Neurofibromatosis, Type II (NF2) approved 101000
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