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.
| Condition name | Status | OMIM number | Documents |
|---|---|---|---|
| Gonadal mosaicism | approved | ||
| Gorlin Syndrome | approved | 109400 | |
| Greig Cephalopolysyndactyly (GCPS) | approved | 175700 | |
| GRN-related Frontotemporal Lobar Degeneration with TDP43 inclusions | approved | 607485 | |
| Haemoglobin SC disease | approved | 141900.0038 | |
| Haemophilia A (HEMA) | approved | 306700 | |
| Haemophilia B (HEMB) | approved | 306900 | |
| Harel-Yoon Syndrome, (HAYOS) | approved | 617183 | |
| Heimler syndrome Type 2 | awaiting approval | 616617 | |
| Hereditary Angioedema (HAE) Type I & Type II | approved | 106100 | |
| Hereditary Angioedema (HAE) Type III | approved | 610618 | |
| Hereditary diffuse gastric cancer (HDGC) | approved | 137215 | |
| Hereditary Emberger Syndrome | approved | 614038 | |
| Hereditary Haemorrhagic Telangiectasia (HTT) or Rendu-Osler-Weber Syndrome | approved | 187300 | |
| Hereditary Haemorrhagic Telangiectasia Type 2 (HHT2) | approved | 600376 | |
| Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) | approved | 150800 | |
| Hereditary motor and sensory neuropathy, type IIc (HMSN2C) | approved | 606071 | |
| Hereditary Multiple Exostoses Type II | approved | 133701 | |
| Hereditary Nonpolyposis Colorectal Cancer: Lynch Syndrome (for all subtypes) | approved | ||
| Hereditary Pancreatitis | approved | 167800 | |