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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
Thrombocytopenia Absent Radius Syndrome awaiting approval 274000
Timothy Syndrome (TS) approved 601005
Townes-Brocks Syndrome approved 107480
TPRN-associated autosomal recessive non-syndromic deafness (DFNB79) approved 613307
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
Usher syndrome type 2 (including subtypes 2A, 2C and 2D) approved 276901, 605472, 611383
Van der Woude syndrome Type 1 approved 119300
Vasculopathy, Retinal, with Cerebral Leukodystrophy (RVCL) approved 192315
Vici syndrome (VICIS) approved 242840
Von Hippel Lindau syndrome (VHL) approved 193300
Waardenburg Syndrome Type I (WS1) approved 193500