Myopathies, Structural, Congenital

Source:http://linkedlifedata.com/resource/umls/id/C0752282

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MSH: A heterogeneous group of diseases characterized by the early onset of hypotonia, developmental delay of motor skills, non-progressive weakness. Each of these disorders is associated with a specific histologic muscle fiber abnormality.,NCI: A group of rare genetic muscle disorders characterized by hypotonia, muscle weakness, and delayed development of motor skills.
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