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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 pgd@hfea.gov.uk.

Condition name Status OMIM number Documents
Hereditary Haemorrhagic Telangiectasia Type 2 (HHT2) approved 600376
Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) approved 150800
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
Hirschsprung Disease 1 (HSCR1) approved 142623
Holt Oram Syndrome approved 142900
Homocystinuria approved 236200
Homozygous familial hypercholesterolaemia approved 143890
Huntington Disease (Huntington Chorea) (HD) approved 143100
Huntington disease-like (HDL1) approved 603218
Hutchinson-Gilford Progeria Syndrome (HGPS) approved 176670
Hyaline Fibromatosis Syndrome (HFS) approved 228600
Hyper IgM Syndrome - Hypogammaglobulinaemia* approved 308230
Hyper-IgE Recurrent Infection Syndrome, Autosomal Dominant approved 147060
Hyperphosphatasia with intellectual disability syndrome 2 approved 614749
Hyperphosphatasia with intellectual disability syndrome 3 approved 614207
Hyperphosphatasia with intellectual disability syndrome 5 approved 616025
Hyperphosphatasia with intellectual disability syndrome 6 approved 616809