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 |
|---|---|---|---|
| Mitochondrial DNA Depletion Syndrome 13 (Encephalomyopathic Type) (MTDPS13) | approved | 615471 | |
| Mitochondrial DNA Depletion Syndrome 15 (Hepatocerebral Type) (MTDPS15) | approved | 617156 | |
| Mitochondrial DNA Depletion Syndrome 2 (myopathic type) (MTDPS2) | approved | 609560 | |
| Mitochondrial DNA Depletion Syndrome 3 (Hepatocerebral Type) (MTDPS3) | approved | 251880 | |
| Mitochondrial DNA depletion syndrome 4A (Alpers type) (MTDPS4A) | approved | 203700 | |
| Mitochondrial DNA Depletion Syndrome 5 (Encephalomyopathic with or without Methylmalonic Aciduria) (MTDPS5) | approved | 612073 | |
| Mitochondrial DNA Depletion Syndrome 6 (Hepatocerebral Type) (MTDPS6) | approved | 256810 | |
| Mitochondrial DNA Depletion Syndrome 7 (Hepatocerebral Type) (MTDPS7) | approved | 271245 | |
| Mitochondrial DNA Depletion Syndrome 8A (Hepatocerebral Type) (MTDPS8A) | approved | 612075 | |
| Mitochondrial DNA Depletion Syndrome 9 (Hepatocerebral Type) (MTDPS9) | approved | 245400 | |
| Mitochondrial Myopathy and Ataxia (MMYAT) (Autosomal Recessive) | approved | 617675 | |
| Mitochondrial Myopathy with Diabetes | approved | 500002 | |
| Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) | approved | 540000 | |
| Mitochondrial Short-Chain Enoyl-CoA Hydratase 1 Deficiency (ECHS1D) | approved | 616277 | |
| Mitochondrial Trifunctional Protein Deficiency 1 (MTPD1) | approved | 609015 | |
| Molybdenum Cofactor Deficiency Type B (MOCODB) | approved | 252160 | |
| Mosaic Variegated Aneuploidy Syndrome 1; MVA1 | awaiting consideration | 257300 | |
| Muckle-Wells Syndrome (MWS) | approved | 191900 | |
| Mucolipidosis II Alpha/Beta | approved | 252500 | |
| Mucolipidosis III Alpha/Beta | approved | 252600 | |
