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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation (disorder)
Clinical finding (finding) > disease > Genetic disease > Congenital myopathy with fibre type disproportion > Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation (disorder)

Preferred term

Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation (disorder)  

Type

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

Associated morphology

Finding site

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/1209168005

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