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bn:00056631n
Noun Concept
SYL
No term available
EN
A mild, rare, congenital form of myotonia characterized by muscle stiffness WordNet 3.0
Relations
Sources
IS A
EN
myotonia
EN
rare disease
EN
channelopathy
HAS KIND
EN
Becker myotonia
EN
Schwartz-Jampel syndrome 1
DRUG USED FOR TREATMENT
EN
ranolazine
GENETIC ASSOCIATION
EN
CLCN1
HEALTH SPECIALTY
EN
neurology
NAMED AFTER
EN
Asmus Julius Thomsen
SYMPTOMS
EN
myotonia

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