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 |
|---|---|---|---|
| Huntington Disease (Huntington Chorea) (HD) | approved | 143100 | |
| Huntington disease-like (HDL1) | approved | 603218 | |
| Hutchinson-Gilford Progeria Syndrome (HGPS) | approved | 176670 | |
| Hyaline Fibromatosis Syndrome (HFS) | approved | 228600 | |
| Hydrocephalus, Congenital, 1 (HYC1) | awaiting consideration | 236600 | |
| Hyper IgM Syndrome - Hypogammaglobulinaemia* | approved | 308230 | |
| Hyper-IgE Recurrent Infection Syndrome, Autosomal Dominant | approved | 147060 | |
| Hyperparathyroidism 1 (HRPT1) | approved | 145000 | |
| Hyperparathyroidism 2 with Jaw Tumors (HRPT2) | approved | 145001 | |
| Hyperparathyroidism 4 (HRPT4) | approved | 617343 | |
| Hyperparathyroidism, Neonatal Severe (NSHPT) | approved | 239200 | |
| Hyperparathyroidism, Transient Neonatal (HRPTTN) | approved | 618188 | |
| Hyperphenylalaninemia, BH4-deficient, A (HPABH4A) | approved | 261640 | |
| Hyperphenylalaninemia, BH4-deficient, B (HPABH4B) | approved | 233910 | |
| Hyperphenylalaninemia, BH4-deficient, C (HPABH4C) | approved | 261630 | |
| Hyperphosphatasia with intellectual disability syndrome 2 | approved | 614749 | |
| Hyperphosphatasia with intellectual disability syndrome 3 | approved | 614207 | |
| Hyperphosphatasia with intellectual disability syndrome 5 | approved | 616025 | |
| Hyperphosphatasia with intellectual disability syndrome 6 | approved | 616809 | |
| Hyperphosphatasia with intellectual disability syndrome 7 | approved | 280000 | |
