Osteogenesis Imperfecta, Type Iv (OI4)

Alias:
Osteogenesis Imperfecta Type 4
Osteogenesis Imperfecta Type Iv
Oi, Type Iv
Oi4
Osteogenesis Imperfecta with Normal Sclerae
Oi Type 4
Osteogenesis Imperfecta with Normal Sclerae, Dominant Form
Osteogenesis Imperfecta with Normal Sclera
Osteogenesis Imperfecta 4
Oi Type Iv
Oi-Iv
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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
成骨不全症,类型IV,也称为成骨不全症类型4,与成骨不全症类型VIII和成骨不全症类型V有关。与成骨不全症,类型IV相关的基因是COL1A2(胶原蛋白Iα2链),其相关通路/超级通路包括细胞外基质组织和ECM蛋白聚糖。在该疾病的背景下,已提到的药物有唑来膦酸和胆骨化醇。相关组织包括骨和眼,相关表型为蓝色巩膜和脊柱侧弯。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
常显
新生儿
1-9/100000
33
442
62

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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