Sclerosteosis 1 (SOST1)

Alias:
Sost1
Cortical Hyperostosis with Syndactyly
Sclerosteosis
Sost
Cortical Hyperostosis Syndactyly
Sclerosteosis, Type 1
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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
Sclerosteosis 1,也被称为 sost1,与范布克病和颅面骨发育不良有关,其症状包括不明原因的视力丧失。与Sclerosteosis 1有关的重要基因是SOST(骨硬化蛋白),其相关通路/超级通路包括维生素D受体通路和RUNX2调节骨骼发育。该病与药物二膦酸盐有关。相关组织包括骨和脑桥,相关表型为前额突出和大脸。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
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12
89
21

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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No data available

Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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No Data Found!
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