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 |
---|---|---|---|
Microcephalic Osteodysplastic Primordial Dwarfism Type 1, (MOPD1) | approved | 210710 | |
Microcephalic Osteodysplastic Primordial Dwarfism Type 2, (MOPD2) | approved | 210720 | |
Microcephaly with or without chorioretinopathy, lymphoedema or mental retardation | approved | 152950 | |
Microcephaly, developmental delay and seizures, associated with homozygous mutations in the CSTB | awaiting approval | 601145 | |
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 | |
Mitochondrial Complex V (ATP synthase) Deficiency, Nuclear Type 2 (MC5DN2) | approved | 614052 | |
Mitochondrial Complex V (ATP synthase) Deficiency, Nuclear Type 5 (MC5DN5) | approved | 618120 | |
Mitochondrial Complex V Deficiency | approved | 604273 | |
Mitochondrial DNA Depletion Syndrome 13 (MTDPS13) | approved | 615471 | |
Mitochondrial DNA Depletion Syndrome 15 (MTDPS15) | approved | 617156 | |
Mitochondrial DNA Depletion Syndrome 2 (myopathic type) (MTDPS2) | approved | 609560 | |
Mitochondrial DNA Depletion Syndrome 3 (MTDPS3) | approved | 251880 | |
Mitochondrial DNA depletion syndrome 4A (Alpers type) (MTDPS4A) | approved | 203700 | |
Mitochondrial DNA Depletion Syndrome 5 (MTDPS5) | approved | 612073 | |
Mitochondrial DNA Depletion Syndrome 6 (MTDPS6) | approved | 256810 | |