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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.

Download full approved condition list.

Condition name Status OMIM number Documents
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
Hereditary Sensory Neuropathy type 1A approved 162400
Hermansky-Pudlak Syndrome 1 (HPS1) approved 203300
Hermansky-Pudlak Syndrome 2 (HPS2) approved 608233
Hermansky-Pudlak Syndrome 3 (HPS3) approved 614072
Hermansky-Pudlak Syndrome 4 (HPS4) approved 614073
Hermansky-Pudlak Syndrome 5 (HPS5) approved 614074
Hermansky-Pudlak Syndrome 6 (HPS6) approved 614075
Hermansky-Pudlak Syndrome 7 (HPS7) approved 614076
Hermansky-Pudlak Syndrome 8 (HPS8) approved 614077
Heterotaxy, Visceral, 7, Autosomal; HTX7 awaiting approval 616749
Hirschsprung Disease 1 (HSCR1) approved 142623
Holt Oram Syndrome approved 142900
Homocystinuria approved 236200