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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 Dominant Intellectual Developmental Disorder 31 (MRD31)
Alias:
Autosomal Dominant Non-Syndromic Intellectual Disability 31
Autosomal Dominant Mental Retardation 31
Mrd31
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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
常染色体显性第31号智力发育障碍,又称常染色体显性非综合征性智力障碍31,与神经发育障碍有关,伴有新生儿呼吸不足、肌张力低下和喂养困难以及旁骨骨肉瘤。与常染色体显性第31号智力发育障碍相关的重要基因是PURA(富含嘌呤元素结合蛋白A),其相关通路/超通路包括染色体组织和胚层化。相关表型为双侧下眼睑外翻和步态宽大。
Related ID:
MALACARDS:ATS527
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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未知
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19
280
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ATS527
Medical Symptom
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Gene & Mutation
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MGI
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