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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
Congenital hereditary cataract, type 44 (CTRCT44) approved 616509
Congenital hereditary cataract, type 6 (CTRCT6) approved 116600
Congenital hereditary cataract, type 9 (CTRCT9) approved 604219
Congenital hypomyelinating neuropathy 1 approved 605253
Congenital hypomyelinating neuropathy 2 approved 618184
Congenital hypomyelinating neuropathy 3 (CHN3) approved 618186
Congenital Mitochondrial Encephalomyopathy approved 500002
Congenital stationary night blindness Type 1A (CSNB1A) approved 310500
Conradi-Hunermann-Happle Syndrome approved 302960
Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis, approved 602066
Cowden syndrome (CS)/PTEN Hamartoma Tumour Syndrome (PHTS) approved 601728, 158350, 153480, 605309
Craniofrontonasal syndrome (CFNS) approved 304110
Crigler-Najjar Syndrome Type 1 (CN1) approved 218800
Crouzon Syndrome approved 123500
Crouzon with acanthosis nigrans syndrome approved 612247
Currarino Syndrome approved 176450
Cutis Laxa, autosomal dominant 1 (ADCL1) approved 123700
Cutis Laxa, autosomal recessive, type IA (ARCL1A) approved 219100
Cutis Laxa, autosomal recessive, type IB (ARCL1B) approved 614437
Cutis Laxa, autosomal recessive, type IC (ARCL1C) approved 613177