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 |
|---|---|---|---|
| Hereditary Nonpolyposis Colorectal Cancer: Lynch Syndrome (for all subtypes) | approved | ||
| Hereditary Pancreatitis | approved | 167800 | |
| Hereditary Sensory Neuropathy type 1A | approved | 162400 | |
| Hermansky-Pudlak Syndrome 1 (HPS1) | approved | 203300 | |
| Hermansky-Pudlak Syndrome 2 (HPS2) | approved | 608233 | |
| Hermansky-Pudlak Syndrome 3 (HPS3) | approved | 614072 | |
| Hermansky-Pudlak Syndrome 4 (HPS4) | approved | 614073 | |
| Hermansky-Pudlak Syndrome 5 (HPS5) | approved | 614074 | |
| Hermansky-Pudlak Syndrome 6 (HPS6) | approved | 614075 | |
| Hermansky-Pudlak Syndrome 7 (HPS7) | approved | 614076 | |
| Hermansky-Pudlak Syndrome 8 (HPS8) | approved | 614077 | |
| Heterotaxy, visceral, 12, autosomal (HTX12) | approved | 619702 | |
| Heterotaxy, visceral, 6, autosomal (HTX6) | approved | 614779 | |
| Heterotaxy, visceral, 7, autosomal (HTX7) | approved | 616749 | |
| Heterotaxy, visceral, 8, autosomal (HTX8) | approved | 617205 | |
| Hirschsprung Disease 1 (HSCR1) | approved | 142623 | |
| Holoprosencephaly 5 (HPE5) | awaiting consideration | 609637 | |
| Holt Oram Syndrome | approved | 142900 | |
| Homocystinuria | approved | 236200 | |
| Homozygous familial hypercholesterolaemia (approved when homozygously inherited but not when heterozygously inherited) | approved | 143890 | |
