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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

Download full approved condition list.

Condition name Status OMIM number Documents
Osteogenesis Imperfecta, Type XIX (OI19) approved 301014
Osteopetrosis with Renal Tubular Acidosis (OPTB3) approved 259730
Osteopetrosis, Autosomal Recessive 5 (OPTB5) and Osteopetrosis, Infantile Malignant 3 approved 259720
Ostheopathia Striata with Cranial Sclerosis (OSCS) approved 300373
Otodental Dysplasia approved 166750
Otopalatodigital syndrome Type 2 (OPD2) approved 304120
Otopalatodigital type 1 approved 311300
Pachyonychia Congenita Type 1 approved 167200
Pachyonychia Congenita Type 2 approved 167210
Pachyonychia Congenita Type 3 approved 615726
Pachyonychia Congenita Type 4 approved 615728
Palmoplantar keratoderma, epidermolytic (EPPK) approved 144200
Palmoplantar keratoderma, non-epidermolytic (NEPPK) approved 600962
Palmoplantar Keratoderma, Nonepidermolytic, Focal or Diffuse approved 615735
Panhypopituitarism, X-linked; PHPX approved 312000
Paragangliomas 4 (PGL4) approved 115310
Paramyotonia Congenita (PMC) approved 168300
Paramyotonia Congenita of von Eulenburg approved 168300
Parathyroid Adenomatosis, Familial Cystic approved 145001
Parkinson’s disease 1 approved 168601