Genetics
Plain-English guides to inherited conditions, genetic testing and how risk is explained in UK genetic services.
42 guides
See also: Pregnancy, Children's health, Lab tests
G
- Gen achondroplasia fgfr3
- Gen becker muscular dystrophy
- Gen beta thalassemia major
- Gen brca1 brca2 breast ovarian cancer
- Gen brugada syndrome scn5a
- Gen color blindness red green
- Gen cowden syndrome pten
- Gen cystic fibrosis cftr mutations
- Gen duchenne muscular dystrophy dmd
- Gen familial adenomatous polyposis
- Gen familial amyloid polyneuropathy
- Gen familial hypercholesterolemia ad
- Gen fragile x syndrome fmr1
- Gen gaucher disease type1
- Gen hemophilia a f8 gene
- Gen hemophilia b f9 gene
- Gen hemophilia c f11
- Gen hereditary spherocytosis spectrin
- Gen huntingtons disease expansion
- Gen hypertrophic cardiomyopathy sarcomeric
- Gen leber hereditary optic neuropathy
- Gen leigh syndrome mitochondrial
- Gen li fraumeni syndrome tp53
- Gen long qt syndrome kvlqt1
- Gen lynch syndrome mismatch repair
- Gen lysinuric protein intolerance
- Gen maple syrup urine disease
- Gen marfan syndrome fibrillin
- Gen merrf myoclonic epilepsy mtdna
- Gen mitochondrial myopathy melas
- Gen mitochondrial neurogastrointestinal
- Gen neurofibromatosis type1 nf1
- Gen osteogenesis imperfecta collagen
- Gen peutz jeghers syndrome stk11
- Gen phenylketonuria pah
- Gen polycystic kidney disease ad
- Gen sickle cell disease hbs
- Gen von hippel lindau vhl
- Gen williams syndrome elastin
- Gen wilson disease atp7b
- Gen x linked adrenoleukodystrophy abcd1
- Gen x linked agammaglobulinemia btk