Skip to main content

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

Download full approved condition list.

Condition name Status OMIM number Documents
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, 12, autosomal (HTX12) approved 619702
Heterotaxy, visceral, 6, autosomal (HTX6) approved 614779
Heterotaxy, visceral, 7, autosomal (HTX7) approved 616749
Heterotaxy, visceral, 8, autosomal (HTX8) approved 617205
Hirschsprung Disease 1 (HSCR1) approved 142623
Holoprosencephaly 5 (HPE5) awaiting consideration 609637
Holt Oram Syndrome approved 142900
Homocystinuria approved 236200
Homozygous familial hypercholesterolaemia (approved when homozygously inherited but not when heterozygously inherited) approved 143890