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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
Alport Syndrome 2, Autosomal Recessive (ATS2)
Alias:
Ats2
Alport Syndrome, Autosomal Recessive
Autosomal Recessive Alport Syndrome
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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
Alport 综合症 2, 常染色体隐性型,也被称为 ats2,与 Alport 综合症 3b, 常染色体隐性和常染色体隐性 Alport 综合症有关。与 Alport 综合症 2, 常染色体隐性型相关的基因是 COL4A4 (IV 型胶原α4链),其相关通路/超通路包括细胞骨架重塑、Rho GTPases 调节的肌动蛋白细胞骨架和非整合素膜-ECM 交互作用。相关组织包括眼睛和肾脏,相关表型包括高血压和听力障碍。
Related ID:
MALACARDS:ALP105
OMIM:203780
MESH:D009394
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
2
19
79
ALP105
Medical Symptom
#
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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