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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
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
Hydrocephalus, Congenital, 1 (HYC1) awaiting consideration 236600
Hyper IgM Syndrome - Hypogammaglobulinaemia* approved 308230
Hyper-IgE Recurrent Infection Syndrome, Autosomal Dominant approved 147060
Hyperparathyroidism 1 (HRPT1) approved 145000
Hyperparathyroidism 2 with Jaw Tumors (HRPT2) approved 145001
Hyperparathyroidism 4 (HRPT4) approved 617343
Hyperparathyroidism, Neonatal Severe (NSHPT) approved 239200
Hyperparathyroidism, Transient Neonatal (HRPTTN) approved 618188
Hyperphenylalaninemia, BH4-deficient, A (HPABH4A) approved 261640
Hyperphenylalaninemia, BH4-deficient, B (HPABH4B) approved 233910
Hyperphenylalaninemia, BH4-deficient, C (HPABH4C) approved 261630
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
Hyperphosphatasia with intellectual disability syndrome 7 approved 280000