Osteoporosis, Childhood- or Juvenile-Onset, with Developmental Delay (OPDD)

Alias:
Opdd
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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
骨质疏松症,儿童或青少年型,伴有发育迟缓,也被称为OPDD。与骨质疏松症,儿童或青少年型,伴有发育迟缓有关的重要基因是COPB2(COPI包被复合物亚基β2)。相关组织包括骨,相关表型为骨质疏松和全球发育迟缓。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
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1
9
1

Medical Symptom

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

Gene & Mutation

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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

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PMID
Journal
Year
IF
No Data Found!
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