Microcephaly-Complex Motor and Sensory Axonal Neuropathy Syndrome

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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
小头症-复合运动和感觉轴突神经病综合症 与小头症-复合运动和感觉轴突神经病综合症有关的重要基因是VRK1(VRK丝氨酸/苏氨酸激酶1)。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
胎儿期
<1/1000000
1
7
1

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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