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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
Gonadal mosaicism approved
Gorlin Syndrome approved 109400
Greig Cephalopolysyndactyly (GCPS) approved 175700
GRN-related Frontotemporal Lobar Degeneration with TDP43 inclusions approved 607485
Haemoglobin SC disease approved 141900.0038
Haemophilia A (HEMA) approved 306700
Haemophilia B (HEMB) approved 306900
Harel-Yoon Syndrome, (HAYOS) approved 617183
Heimler syndrome Type 2 awaiting approval 616617
Hereditary Angioedema (HAE) Type I & Type II approved 106100
Hereditary Angioedema (HAE) Type III approved 610618
Hereditary diffuse gastric cancer (HDGC) approved 137215
Hereditary Emberger Syndrome approved 614038
Hereditary Haemorrhagic Telangiectasia (HTT) or Rendu-Osler-Weber Syndrome approved 187300
Hereditary Haemorrhagic Telangiectasia Type 2 (HHT2) approved 600376
Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) approved 150800
Hereditary motor and sensory neuropathy, type IIc (HMSN2C) approved 606071
Hereditary Multiple Exostoses Type II approved 133701
Hereditary Nonpolyposis Colorectal Cancer: Lynch Syndrome (for all subtypes) approved
Hereditary Pancreatitis approved 167800