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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Congenital fibre-type disproportion myopathy due to ACTA1 mutation
Clinical finding (finding) > disease > Genetic disease > Congenital myopathy with fibre type disproportion > Congenital fibre-type disproportion myopathy due to ACTA1 mutation

Preferred term

Congenital fibre-type disproportion myopathy due to ACTA1 mutation  

Type

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

Associated morphology

Finding site

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/1208413008

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