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 pgtm@hfea.gov.uk.

Download full approved condition list.

Condition name Status OMIM number Documents
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
Cerebral Cavernous Malformations 3 (CCM3) approved 603285
Cerebral Creatine Deficiency Syndrome 1 (CCDS1) approved 300352
Cerebral Creatine Deficiency Syndrome 2 (CCDS2) approved 612736
Cerebral Creatine Deficiency Syndrome 3 (CCDS3) approved 612718
Cerebro-oculo-facial-skeletal syndrome Type 1 (COFS1) approved 214150
Cerebro-oculo-facial-skeletal syndrome Type 2 (COFS2) approved 610756
Cerebro-oculo-facial-skeletal syndrome Type 3 (COFS3) approved 616570
Cerebro-oculo-facial-skeletal syndrome type 4 (COFS4) approved 610758
Ceroid Lipofuscinosis, Neuronal, type 1 (CLN1) approved 256730
Ceroid Lipofuscinosis, Neuronal, type 1 (CLN1) approved 256740
Ceroid Lipofuscinosis, Neuronal, type 10 (CLN10) approved 610127
Ceroid Lipofuscinosis, Neuronal, Type 2 (CLN2) approved 204500
Ceroid Lipofuscinosis, Neuronal, type 5 (CLN5) approved 256731