Craniosynostosis 1 (CRS1)

Alias:
Congenital Rubella Syndrome
Crs
Craniostenosis
Mother-to-Child Transmission of Rubella Syndrome
Craniosynostosis, Type 1
Fetal Rubella Syndrome
Congenital Rubella
Crs1
Twist1-Related Craniosynostosis
Rubella, Congenital
Craniosynostosis
Gregg 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
颅缝早闭1,又称先天性风疹综合征,与颅缝早闭和缝合有关。与颅缝早闭1有关的重要基因是TWIST1(扭曲家族BHLH转录因子1)。在该疾病的背景下提到了药物氨甲环酸和凝血剂。附属组织包括大脑和眼睛,相关表型为白内障和感音神经性听力障碍。
Related ID:
MESH:D003398
ICD11:1059053724

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
胎儿期
<1/1000000
2
19
65

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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