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SCN4A-related myopathy, autosomal recessive

Disease Summary
Associated Targets (5)
Tbio

4

Tclin

1


Mondo Description Any congenital myopathy in which the cause of the disease is a mutation in the SCN4A gene. It include is a spectrum of autosomal recessive disorders including congenital myasthenic syndrome, fetal hypokinesia, and congenital myopathy.
Mondo Term and Equivalent IDs
MONDO:0100121:  SCN4A-related myopathy, autosomal recessive