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Congenital myotonia, autosomal dominant form (disorder)
Congenital myotonia, autosomal dominant form
Thomsen myotonia congenita
Myotonia congenita - autosomal dominant form
Thomsen's disease
myotonia congenita Thomsen-type
autosomaal dominante congenitale myotonie
Id57938005
StatusPrimitive
Dutch rare neuromuscular disorders simple reference set
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG71.1
RuleTRUE
AdviceALWAYS G71.1
CorrelationSNOMED CT source code to target map code correlation not specified