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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
Charcot-Marie-Tooth Disease, Axonal, Type 2q (CMT2Q)
Alias:
Charcot-Marie-Tooth Disease Axonal Type 2q
Cmt2q
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2q
Charcot-Marie-Tooth Neuropathy, Type 2q
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2q
Autosomal Dominant Axonal Charcot-Marie-Tooth Disease Type 2q
Charcot-Marie-Tooth Disease Axonal Autosomal Dominant Type 2q
Charcot-Marie-Tooth Neuropathy Axonal Type 2q
Charcot-Marie-Tooth Disease, Axonal, 2q
Charcot-Marie-Tooth Neuropathy Type 2q
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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
Charcot-Marie-Tooth病,轴突型2q,也称为Charcot-Marie-Tooth病轴突型2q,与Charcot-Marie-Tooth病和聋病以及Charcot-Marie-Tooth病有关。Charcot-Marie-Tooth病,轴突型2q的一个重要基因是DHTKD1(脱氢酶E1和酮糖脱氢酶域含1),其相关通路/超级通路包括SLITs和ROBOs表达的调节和糖酵解(BioCyc)。附属组织包括骨骼肌,相关表型为骨骼肌萎缩和足内翻。
Related ID:
MALACARDS:CHR489
OMIM:615025
MESH:D002607
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
青少年
<1/1000000
9
50
2
CHR489
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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