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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
Arthrogryposis Distal type 5 (DA5) approved 108145
Arthrogryposis Distal type 5D (DA5D) approved 615065
Arthrogryposis Distal type 7 (DA7) approved 158300
Arthrogryposis Distal type 8 (DA8) approved 178110
Arthrogryposis multiplex congenita, distal, type 2B approved 601680
Arthrogryposis renal dysfunction and cholestasis Types 1 and 2 approved 208085, 613404
Ataxia Telangiectasia approved 208900
Atrial Septal Defect (ASD) 7 with or without motor conduction defects approved 108900
Atypical Haemolytic Uraemic Syndrome Type 1 awaiting approval 235400
Autosomal Dominant Acute Necrotizing Encephalopathy approved 608033
Autosomal dominant Dyskeratosis Congenita 1 (DKCA1) due to TERC mutation approved 127550
Autosomal dominant familial exudative vitreoretinopathy types 1, 4 and 5 approved 133780, 613310, 601813
Autosomal Dominant Polycystic Kidney Disease 1 (APKD1) approved 173900
Autosomal Dominant Polycystic Kidney Disease type 2 (ADPKD2) awaiting approval 613095
Autosomal Dominant Retinitis Pigmentosa (AP37) approved 611131
Autosomal Dominant Retinitis Pigmentosa Type 4 approved 613731
Autosomal dominant vitreoretinochoroidopathy approved 193220
Autosomal recessive bestrophinopathy approved 611809
Autosomal recessive congenital hyperinsulinism approved 256450, 601820
Autosomal recessive Deafness Type 1A (DFNB1A) approved 220290