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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
罕见病
Aceruloplasminemia (ACERULOP)
Alias:
Cerebellar Ataxia
Hemosiderosis, Systemic, Due to Aceruloplasminemia
Hereditary Ceruloplasmin Deficiency
Deficiency of Ferroxidase
Hypoceruloplasminemia
Familial Apoceruloplasmin Deficiency
Hypoceruloplasminemia, Hereditary
Systemic Hemosiderosis Due to Aceruloplasminemia
Ceruloplasmin Deficiency
Acerulop
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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
阿克瑟乌普拉斯明血症,又称小脑性共济失调,与脊髓小脑性共济失调、常染色体隐性8型和常染色体显性小脑性共济失调有关,症状包括共济失调、斜颈和齿轮样强直。与阿克瑟乌普拉斯明血症有关的重要基因是CP(铜蓝蛋白),其相关通路/超级通路包括2型糖尿病。在该疾病的背景下,已提到的药物有氯硝西泮和聚雌二醇磷酸盐。附属组织包括脂肪、眼睛和大脑,相关表型为神经系统异常和低色素性小细胞性贫血。
Related ID:
MALACARDS:ACR006
OMIM:604290
MESH:D019189
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
成年期
<1/1000000
107
1011
67
ACR006
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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