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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

Condition name Status OMIM number Documents
X-linked Cardiac Valvular Dysplasia approved 314400
X-linked Chronic Granulomatous Disease (CGDX) approved 306400
X-linked Ectodermal dysplasia 1 (Hypohidrotic) approved 305100
X-linked heterotaxy 1 (HTX1) - ZIC3 associated congenital heart defects and heterotaxy approved 306955
X-linked Hydrocephalus (HSAS) approved 307000
X-linked lissencephaly approved 300067
X-Linked Lymphoproliferative Disease Type 2 (XLP2) (Male Embryos Only) approved 300365
X-linked Ocular Albinism approved 300500
X-linked Opitz GBBB syndrome Type 1 approved 300000
X-linked panhypopituitarism awaiting approval 312000
X-Linked Reducing Body Myopathy - severe infantile/early childhood onset approved 300717
X-linked Retinoschisis (RS1) approved 312700
X-Linked Thrombocytopenia (XLT) approved 313900
XMEN syndrome (X Linked magnesium defect, EBV, neoplasia) approved 300853