登记Id

PA445032

基因名称(英)

Myotonia Congenita

别名

"Becker Generalized Myotonia","Generalized Myotonia","Generalized Myotonia of Becker","Generalized Myotonia of Thomsen","Generalized Myotonia, Becker","Generalized Myotonias","Myotonia Levior","Myotonia, Becker Generalized","Myotonia, Generalized","Myotonia, Generalized, Becker","Myotonias, Generalized","Thomsen Disease","Thomsen Generalized Myotonia","Thomsen Generalized Myotonias","Thomsen's Disease","Thomsen's disease","Thomsens Disease"

交叉引用

外部词汇

"MeSH:D009224(Myotonia Congenita)","SnoMedCT:57938005(Congenital myotonia, autosomal dominant form)","UMLS:C0027127(C0027127)","MedDRA:10028655(Myotonia congenita)","NDFRT:N0000002098(Myotonia Congenita [Disease/Finding])"