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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
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2l
Alias:
Muscular Dystrophy, Limb-Girdle, Type 2l
Lgmd2l
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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
常染色体隐性肢带型肌肉萎缩症21型,也称为肌肉萎缩症、肢带型21型,与下颌骨发育不良和宫崎肌肉萎缩症3有关,症状包括肌肉疼痛。与常染色体隐性肢带型肌肉萎缩症21型相关的重要基因是ANO5(无孔蛋白5),其相关通路/超通路包括DREAM抑制和杜氏醇表达和糖基化疾病。相关组织包括骨骼肌和骨,相关表型为肌肉和稳态/代谢。
Related ID:
MALACARDS:ATS217
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
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Reference
MALACARDS
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未知
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16
125
53
ATS217
Medical Symptom
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Gene & Mutation
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Name
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Category
Name
MGI
Related Gene
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