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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
Immunodeficiency, common variable, 12, with autoimmunity (CVID12) approved 616576
Immunodeficiency, common variable, 13, with autoimmunity (CVID13) approved 616873
Immunodeficiency, common variable, 2, with autoimmunity (CVD2) (autosomal recessive form only) approved 240500
Immunodeficiency, common variable, 3, with autoimmunity (CVID3) approved 613493
Immunodeficiency, common variable, 8, with autoimmunity (CVID8) approved 614700
Inclusion Body Myopathy with early onset Paget Disease and Frontotemporal Dementia 1 (IBMPFD1) approved 167320
Incontinentia Pigmenti (IP) approved 308300
Inflammatory Bowel Disease, Early-onset (IBD25) approved 612567
Inflammatory Bowel Disease, Early-onset (IBD28) approved 613148
Inherited Erythromelalgia (IEM) approved 133020
Intellectual Development Disorder, autosomal dominant, 29 (MRD29) approved 616078
Intellectual developmental disorder, X-linked 1 (IQSEC2) approved 309530
Intellectual Disability, Autosomal Recessive 12 approved 611090
Intellectual Disability, X-linked 102 (MRX102) approved 300958
IPEX Syndrome (Immunodeficiency, Polyendocrinopathy and Enteropathy, X-Linked) approved 304790
Isolated Growth Hormone Deficiency - type 1A (IGHD1A) approved 262400
Isolated Microphthalmia 2 (MCOP2) approved 610093
Isolated Sulfite Oxidase Deficiency (ISOD) approved 272300
Jackson Weiss syndrome, OMIM approved 123150
Jalili Syndrome approved 217080