PGD conditions
This table shows all PGD 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 pgd@hfea.gov.uk.
| Condition name | Status | OMIM number | Documents |
|---|---|---|---|
| Temtamy syndrome | awaiting approval | 218340 | |
| Thiamine Metabolism Dysfunction Syndrome 2 | approved | 607196 | |
| Thiamine Metabolism Dysfunction Syndrome 3 | approved | 607196 | |
| Thiamine Metabolism Dysfunction Syndrome 5 | approved | 614458 | |
| Thiamine-responsive Megaloblastic Anaemia | approved | 249270 | |
| Thrombocytopenia Absent Radius (TAR) Syndrome | approved | 274000 | |
| Timothy Syndrome (TS) | approved | 601005 | |
| Townes-Brocks Syndrome | approved | 107480 | |
| TPRN-associated autosomal recessive non-syndromic deafness (DFNB79) | approved | 613307 | |
| Transcobalamin II Deficiency | awaiting approval | 275350 | |
| Treacher Collins Syndrome 1 (TCS1) | approved | 154500 | |
| Treacher Collins Syndrome Type 2 (TCS2) | approved | 613717 | |
| Trichorhinophalangeal syndrome type 1 | approved | 190350 | |
| Tuberous Sclerosis (TSC1 and TSC2) | approved | 191100, 613254 | |
| Turner syndrome (Mosaic) | approved | ||
| Tyrosinaemia Type 1 | approved | 276700 | |
| Tyrosine Hydroxylase Deficiency | approved | 605407 | |
| UBE2A - Intellectual Disability type Nascimento - X linked | approved | 300860 | |
| Ullrich Congenital Muscular Dystrophy 1 (UCMD1) | approved | 254090 | |
| Usher syndrome type 1 (including subtypes 1B, 1C, 1D, 1F, 1G, 1J) | approved | 276900 276904 601067 602083 606943 614869 | |