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 |
|---|---|---|---|
| Neurodegeneration with Brain Iron Accumulation 5 (NBIA5) | approved | 300894 | |
| Neurodegeneration with Brain Iron Accumulation 6 (NBIA6) | approved | 615643 | |
| Neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism (NEDCAFD) | approved | 619244 | |
| Neurodevelopmental disorder with impaired speech and hyperkinetic movements | awaiting approval | #618425 | |
| Neurodevelopmental disorder with impaired speech and hyperkinetic movements (NEDISHM) | approved | 618425 | |
| Neurodevelopmental Disorder with Progressive Microcephaly Spasticity and Brain Anomalies (NDMSBA) | approved | 617527 | |
| Neurofibromatosis type 1 (NF1) | approved | 162200 | |
| Neurofibromatosis Type 2 (NF2) | approved | 101000 | |
| Neurogenic muscle weakness, Ataxia, Retinitis Pigmentosa (NARP) | approved | 551500 | |
| Neuronal Ceroid Lipofuscinosis Type 3 (Batten disease) (CLN3) | approved | 204200 | |
| Neuronopathy Distal Hereditary Motor, Type 2C (HMN2C) | approved | 613376 | |
| Neuronopathy Distal Hereditary Motor, Type 2D (HMN2D) | approved | 615575 | |
| Neuronopathy Distal Hereditary Motor, Type 5A (HMN5A) | approved | 600794 | |
| Neuronopathy Distal Hereditary Motor, Type 5B (HMN5B) | approved | 614751 | |
| Neuronopathy Distal Hereditary Motor, Type 5C (HMN5C) | approved | 619112 | |
| Neuronopathy Distal Hereditary Motor, Type 7A (HMN7A) | approved | 158580 | |
| Neuronopathy Distal Hereditary Motor, Type 7B (HMN7B) | approved | 607641 | |
| Neuronopathy Distal Hereditary Motor, Type IX (HMN9) | approved | 617721 | |
| Neuronopathy, distal hereditary motor, type VIII (HMN8) | approved | 600175 | |
| Neuropathy, distal hereditary motor, type IIA (HMN2A) | approved | 158590 | |