Spondyloperipheral Dysplasia (SPD)

Alias:
Spondyloperipheral Dysplasia-Short Ulna Syndrome
Spondyloperipheral Dysplasia with Short Ulna
Spondyloperipheral Dysplasia Short Ulna
Spd
Dysplasia, Spondyloperipheral
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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
脊旁外周发育不良,也称为spd,与平坦脊柱性致命骨骼发育不良、特兰斯类型和感觉神经性听力损失有关。与脊旁外周发育不良有关的重要基因是COL2A1(胶原蛋白IIα1链),其相关通路/超级通路包括ERK信号通路和整合素通路。附属组织包括骨,相关表型为听力障碍和腭裂。

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
新生儿
<1/1000000
8
65
12

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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