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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
Carpenter Syndrome 2 approved 614976
Cartilage-Hair Hypoplasia approved 250250
Cartilage-hair hypoplasia spectrum approved 157660
Cataract 1 (CTRCT1) approved 116200
Cataract 2 (CTRCT2) approved 604307
Cataract 4 (CTRCT4) approved 115700
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT1) approved 604772
Catecholaminergic Polymorphic Ventricular Tachycardia type 3 (CPVT3) approved 614021
Catecholaminergic Polymorphic Ventricular Tachycardia type 4 (CPVT4) approved 614916
Catecholaminergic Polymorphic Ventricular Tachycardia type 5 with or without muscle weakness (CPVT5) approved 615441
Catecholaminergic Polymorphic Ventricular Tachychardia 2 (CPVT2) approved 611938
Central Core Disease of Muscle (CCD) approved 117000
Central Hypoventilation Syndrome, Congenital, 1 (CCHS1) approved 209880
Centronuclear Myopathy (CNM1) approved 160150
Cerebellar Ataxia, Intellectual Disability and Dysequilibrium Syndrome Type 1 approved 224050
Cerebellar Ataxia, Intellectual Disability and Dysequilibrium Syndrome Type 2 approved 610185
Cerebellar Ataxia, Intellectual Disability and Dysequilibrium Syndrome Type 3 approved 613227
Cerebellar Ataxia, Intellectual Disability and Dysequilibrium Syndrome Type 4 approved 615268
Cerebral Autosomal Dominant Arteriopathy with Sub cortical infarcts and Leukoencephalopathy (CADASIL) approved 125310
Cerebral Cavernous Malformations (CCM) approved 116860