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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
Peripheral Neuropathy with Variable Spasticity, Exercise Intolerance, and Developmental Delay (PNSED)
Alias:
Combined Oxidative Phosphorylation Defect Type 26
Combined Oxidative Phosphorylation Deficiency 26
Coxpd26
Pnsed
Oxidative Phosphorylation Deficiency, Combined, Type 26
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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
可变性痉挛性周围神经病、运动耐受性差和发育延迟,也称为联合氧化磷酸化缺陷型26,与联合氧化磷酸化缺陷和痉挛性双下肢有关。与可变性痉挛性周围神经病、运动耐受性差和发育延迟有关的重要基因是TRMT5(tRNA甲基转移酶5),其相关通路/超级通路包括胚胎和诱导多能干细胞和特异性标记物。附属组织包括胰腺和肾脏,相关表型为痉挛和肌肉无力。
Related ID:
MALACARDS:PRP109
OMIM:616539
MESH:D028361
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
婴儿期
<1/1000000
7
49
5
PRP109
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
Gene
Function
Score
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
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