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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 Charcot-Marie-Tooth disease type 2 > Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation

Preferred term

Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation  

Type

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

Broader concept

Associated morphology

Finding site

Is a

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URI

http://www.irandoc.acir/onto/irandoc/764730007

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