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
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| Id | 57938005 | Status | Primitive |
Dutch rare neuromuscular disorders simple reference set |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | G71.1 | Rule | TRUE | Advice | ALWAYS G71.1 | Correlation | SNOMED CT source code to target map code correlation not specified |
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