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[Paramyotonia congenita]. 2001

K Yoshida, and Y Fukushima
Division of Clinical and Molecular Genetics, Shinshu University Hospital.

UI MeSH Term Description Entries
D008297 Male Males
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D020967 Myotonic Disorders Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) or occur as a generalized condition. Myopathies, Myotonic,Myotonia Fluctuans,Paramyotonia Congenita,Eulenburg Disease,Eulenburg's Disease,Paralysis Periodica Paramyotonia,Paramyotonia Congenita Without Cold Paralysis,Paramyotonia Congenita of von Eulenberg,Von Eulenberg's Disease,Disorder, Myotonic,Disorders, Myotonic,Myopathy, Myotonic,Myotonic Disorder,Myotonic Myopathies,Myotonic Myopathy,Von Eulenberg Disease

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