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Biological Sciences and Healthcare, part 4

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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Desmin-related myofibrillar myopathy (disorder)
... > Clinical finding (finding) > Musculoskeletal system finding > Disease of the musculoskeletal system, NOS > Disorder of muscle > Myofibrillar myopathy > Desmin-related myofibrillar myopathy (disorder)
... > Clinical finding (finding) > disease > Disorder of body system > Disease of the musculoskeletal system, NOS > Disorder of muscle > Myofibrillar myopathy > Desmin-related myofibrillar myopathy (disorder)
... > Clinical finding (finding) > Musculoskeletal system finding > Disease of the musculoskeletal system, NOS > Disorder of muscle > Congenital anomaly of skeletal muscle > Myopathy with cytoplasmic inclusions > Desmin-related myofibrillar myopathy (disorder)
... > Clinical finding (finding) > disease > Disorder of body system > Disease of the musculoskeletal system, NOS > Disorder of muscle > Congenital anomaly of skeletal muscle > Myopathy with cytoplasmic inclusions > Desmin-related myofibrillar myopathy (disorder)

Preferred term

Desmin-related myofibrillar myopathy (disorder)  

Type

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

Broader concept

Associated morphology

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Is a

Occurrence

Pathological process

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URI

http://www.irandoc.acir/onto/irandoc/770627003

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