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PGD conditions

This table shows all PGD 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 pgd@hfea.gov.uk.

Condition name Status OMIM number Documents
Menkes disease approved 309400
Mental Retardation, X-linked, Syndromic 34, caused by NONO gene mutation (MRXS34) approved 300967
Merosin Deficient Congenital Muscular Dystrophy type 1A (MDC1A) (also known as LAMA2-related Muscular Dystrophy) approved 607855
Metachromatic Leukodystrophy (MLD) approved 250100
Metaphyseal Dysplasia without Hypotrichosis approved 250460
Methylmalonic Acidemia (MMA) approved 251000
Methylmalonic Acidemia cb1A approved 251100
Methylmalonic Acidemia cb1B approved 251110
Methylmalonic Aciduria and Homocystinuria approved 277400
Micro Syndrome (WARBM) approved 600118
Microcephalic Osteodysplastic Primordial Dwarfism Type 1, (MOPD1) approved 210710
Microcephalic Osteodysplastic Primordial Dwarfism Type 2, (MOPD2) approved 210720
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICAL MALFORMATIONS; MCPH2 awaiting approval 604317
Microcephaly with or without chorioretinopathy, lymphoedema or mental retardation approved 152950
Microcephaly, Short Stature and Polymicrogyria with or without seizures (MSSP) approved 614833
Mismatch Repair Cancer Syndrome (MMRCS) approved 276300
Mitochondrial Complex 1 Deficiency caused by mutation in ACAD9 gene approved 611126
Mitochondrial Complex II Deficiency approved 252011
Mitochondrial Complex III Deficiency approved 124000
Mitochondrial Complex IV Deficiency approved 220110