Spastic Paraplegia 76, Autosomal Recessive (SPG76)

Alias:
Autosomal Recessive Spastic Paraplegia Type 76
Spg76
Hereditary Spastic Paraplegia 76
Paraplegia, Spastic, Autosomal Recessive, Type 76
Autosomal Recessive Spastic Paraplegia 76
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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
遗传性痉挛性截瘫76型,常染色体隐性,也称为常染色体隐性痉挛性截瘫76型,与geleophysic dysplasia 3和geleophysic dysplasia有关。与遗传性痉挛性截瘫76型,常染色体隐性相关的基因是CAPN1(钙蛋白酶1),其相关通路/超级通路包括ERK信号通路和Akt信号通路。相关组织包括骨骼肌和眼睛,相关表型为巴宾斯基征和下肢痉挛。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
成年期
<1/1000000
11
149
3

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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