Hereditary Motor and Sensory Neuropathy V (HMSN5)

Alias:
Hmsn V
Charcot-Marie-Tooth Disease-Pyramidal Features Syndrome
Hereditary Motor and Sensory Neuropathy Type 5
Hereditary Motor and Sensory Neuropathy Type V
Hmsn 5
Charcot-Marie-Tooth Neuropathy with Pyramidal Features, Autosomal Dominant
Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant
Peroneal Muscular Atrophy with Pyramidal Features, Autosomal Dominant
Charcot-Marie-Tooth Disease Type 5
Spastic Paraplegia, Hereditary
Cmt with Pyramidal Features
Hmsn5
Favorite
基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
遗传性运动和感觉神经病V,也称为hmsn v,与Charcot-Marie-Tooth病类型5和Charcot-Marie-Tooth病,X连锁隐性,5有关,其症状包括腿部抽筋和下肢疼痛。与遗传性运动和感觉神经病V有关的重要基因是MFN2(融合蛋白2)。在该疾病的背景下,已提到的药物包括乙酰胆碱和胆碱能药物。附属组织包括脊髓,相关表型为痉挛和远端肌肉无力。

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
成年期
--
1
12
9

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!
微信
信息比对
科研助手
使用教程
回到顶部