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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
Optic Atrophy 8 (OPA8)
Alias:
Opa8
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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
视神经萎缩8,也称为opa8,与视神经萎缩有关,伴有或不伴有耳聋、眼肌麻痹、肌病、共济失调和神经病,以及视神经萎缩1。与视神经萎缩8有关的重要基因是OPA8(视神经萎缩8(常染色体显性)),其相关通路/超通路包括伴侣蛋白介导的蛋白质折叠。相关组织包括骨骼肌,相关表型包括二尖瓣反流和中心性视野缺损。
Related ID:
MALACARDS:OPT060
OMIM:616648
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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OPT060
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HPO Frequency
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MGI
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