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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 42 (RP42)
Alias:
Rp42
Retinitis Pigmentosa, Type 42
Retinitis Pigmentosa-42
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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
视网膜色素变性42,也称为rp42,与发育性和癫痫性脑病11以及冷诱导出汗综合征3有关。与视网膜色素变性42相关的基因是KLHL7(Kelch Like Family Member 7),其相关通路/超级通路包括纤毛景观。相关组织包括视网膜和眼睛,相关表型为视力下降和视杆-视锥性色素变性。
Related ID:
MALACARDS:RTN149
OMIM:612943
MESH:C567854
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
--
10
46
5
RTN149
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
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Gene
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Mutations
No data available
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Phase
No data available
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Category
Name
MGI
Related Gene
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