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Biological Sciences and Healthcare, part 5

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Concept information

... > 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

Preferred term

Autosomal dominant congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation  

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  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

Broader concept

Associated morphology

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http://www.irandoc.acir/onto/irandoc/1208418004

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