Hyperphosphatasia with Impaired Intellectual Development Syndrome (HPMRS)

Alias:
Hyperphosphatasia with Mental Retardation Syndrome
Hyperphosphatasia with Mental Retardation
Mabry Syndrome
Mabry Disease
Hpmrs
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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
超磷酸酶血症伴智力障碍综合征,又称超磷酸酶血症伴智力障碍综合征1和超磷酸酶血症-智力障碍综合征。与超磷酸酶血症伴智力障碍综合征相关的重要基因是PGAP2(Post-GPI Attachment To Proteins 2),其相关通路/超级通路包括翻译后修饰:GPI锚定蛋白的合成。附属组织包括心脏和骨骼,相关表型包括上睑裂斜和薄上唇红唇。
Related ID:
MESH:C565495

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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未知
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5
20
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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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