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

Preferred term

Autosomal dominant congenital fibre-type disproportion myopathy due to selenoprotein N mutation  

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

Broader concept

Associated morphology

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Is a

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Pathological process

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URI

http://www.irandoc.acir/onto/irandoc/1202024009

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