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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
Chromosome 17q12 Deletion Syndrome
Alias:
17q12 Microdeletion Syndrome
Monosomy 17q12
Del(17)(q12)
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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
17q12缺失综合症,也被称为17q12微缺失综合症,与17q12重复综合症和梅耶-罗克坦斯基-库斯特-哈乌尔综合症有关。与17q12缺失综合症有关的重要基因是DEL17Q12(17q12缺失综合症),其相关通路/超级通路包括17q12拷贝数变异综合症和肾细胞线粒标记物。附属组织包括肾脏和肝脏,相关表型包括多囊肾发育不良和糖尿病。
Related ID:
MALACARDS:CHR501
OMIM:614527
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
1-9/1000000
15
69
10
CHR501
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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