肌阵挛性癫痫,进行性
登记Id
PA446925
基因名称(英)
Myoclonic Epilepsies, Progressive
别名
"Action Myoclonus Renal Failure Syndrome","Action Myoclonus-Renal Failure Syndrome","Atrophies, Dentatorubral-Pallidoluysian","Atrophy, Dentatorubral-Pallidoluysian","Atypical Inclusion Body Disease","Atypical Inclusion-Body Disease","Atypical Inclusion-Body Diseases","Biotin Responsive Encephalopathy","Biotin-Responsive Encephalopathies","Biotin-Responsive Encephalopathy","Dentatorubral Pallidoluysian Atrophy","Dentatorubral-Pallidoluysian Atrophies","Dentatorubral-Pallidoluysian Atrophy","Disease, Atypical Inclusion-Body","Diseases, Atypical Inclusion-Body","Encephalopathies, Biotin-Responsive","Encephalopathy, Biotin-Responsive","Epilepsies, Progressive Myoclonic","Epilepsies, Progressive Myoclonus","Epilepsy, Progressive Myoclonic","Epilepsy, Progressive Myoclonus","Familial Progressive Myoclonic Epilepsy","Inclusion-Body Disease, Atypical","Inclusion-Body Diseases, Atypical","May White Syndrome","May-White Syndrome","May-White Syndromes","Myoclonic Epilepsy, Progressive","Myoclonus Epilepsies, Progressive","Myoclonus Epilepsy, Progressive","Progressive Myoclonic Epilepsies","Progressive Myoclonic Epilepsy","Progressive Myoclonus Epilepsies","Progressive Myoclonus Epilepsy","Progressive myoclonic epilepsy","Syndrome, May-White","Syndromes, May-White"
交叉引用
外部词汇
"MeSH:D020191(Myoclonic Epilepsies, Progressive)","SnoMedCT:267581004(Progressive myoclonic epilepsy)","UMLS:C0751778(C0751778)","NDFRT:N0000004030(Myoclonic Epilepsies, Progressive [Disease/Finding])"
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