Biological Sciences and Healthcare, part 5

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Autosomal dominant congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation > Autosomal dominant congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation

... > Clinical finding (finding) > disease > Genetic disease > Congenital myopathy with fibre type disproportion > Congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation > Autosomal dominant congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation