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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
Joubert Syndrome 18 (JBTS18)
Alias:
Jbts18
Joubert Syndrome, Type 18
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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
Joubert 综合征 18,也称为 jbts18,与口腔面部数字综合征 IV 和完全异常肺静脉回流 1 有关。与 Joubert 综合征 18 有关的重要基因是 TCTN3(Tectonic 家族成员 3),其相关通路/超级通路包括中胚层承诺通路。附属组织包括肾脏和眼睛,相关表型为后轴多指和枕部脑裂。
Related ID:
MALACARDS:JBR021
OMIM:614815
MESH:D002526
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
6
32
5
JBR021
Medical Symptom
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Categorization
Description
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Orphanet Frequency
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No data available
Gene & Mutation
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No data available
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Name
MGI
Related Gene
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Publications
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References Literature
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