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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
罕见病
Congenital Myopathy 1a, Autosomal Dominant, with Malignant Hyperthermia (CMYP1A)
Alias:
Congenital Myopathy 1a, Autosomal Dominant, with Susceptibility to Malignant Hyperthermia
Central Core Disease of Muscle
Central Core Myopathy
Cmyp1a
Ccd
Moderate Multiminicore Disease with Hand Involvement
Central Core Disease
Cco
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
先天性肌病1a,常染色体显性,伴有恶性高热,也称为先天性肌病1a,常染色体显性,伴有恶性高热易感性,与金登堡综合症和先天性肌病1b,常染色体隐性有关,症状包括全身肌肉无力。与先天性肌病1a,常染色体显性,伴有恶性高热有关的重要基因是RYR1(ryanodine receptor 1)。相关组织包括骨骼肌和皮肤,相关表型为面瘫和新生儿低张力。
Related ID:
MALACARDS:CNG637
OMIM:117000
MESH:D020512
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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未知
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1
24
69
CNG637
Medical Symptom
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Gene & Mutation
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Gene
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Name
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