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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
Retinitis Pigmentosa 67 (RP67)
Alias:
Rp67
Retinitis Pigmentosa, Type 67
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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
Retinitis Pigmentosa 67,也被称为rp67,与 Noonan 综合征伴有多发性色素痣和乳腺腺癌有关。与Retinitis Pigmentosa 67相关的基因是NEK2(NIMA相关激酶2),其相关通路/超级通路包括Sertoli-Sertoli细胞连接动力学和细胞骨架重塑,Rho GTPases调节的肌动蛋白细胞骨架。相关组织包括视网膜和眼睛,相关表型包括杆-锥性视网膜病变和端粒酶活性增加。
Related ID:
MALACARDS:RTN140
OMIM:615565
MESH:D012174
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
5
49
2
RTN140
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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IF
No Data Found!
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