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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
Werner Syndrome (WRN) approved 277700
Wiscott-Aldrich Syndrome (WAS)* approved 301000
Wolcott-Rallison Syndrome approved 226980
Wolfram-like Syndrome (WLS) approved 614296
Wolman's Disease (Acid Lipase Deficiency) approved 278000
Woodhouse-Sakati Syndrome approved 241080
X Linked Periventricular Heterotopia (PVNH1) approved 300049
X-linked Adrenal Hypoplasia Congenita (XL-AHC) approved 300200
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 Reducing Body Myopathy - severe infantile/early childhood onset approved 300717
X-linked Retinoschisis (RS1) approved 312700
X-Linked Thrombocytopenia (XLT) approved 313900