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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
非罕见病
Gillessen-Kaesbach-Nishimura Syndrome (GIKANIS)
Alias:
Polycystic Kidney Disease, Autosomal Recessive, with Microbrachycephaly, Hypertelorism, and Brachymelia
Gikanis
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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
吉列森-凯斯巴赫-西村综合症,又称常染色体隐性多囊肾病伴小头畸形、眼距增宽和短肢,与伴有或不伴有肝多囊病和室间隔缺损的多囊肾病有关。与吉列森-凯斯巴赫-西村综合症相关的重要基因是ALG9(ALG9 Alpha-1,2-Mannosyltransferase)。相关组织包括肾和肺,相关表型为短颈和光滑的鼻唇沟。
Related ID:
MALACARDS:GLL035
OMIM:263210
MESH:D004480
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
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1
3
4
GLL035
Medical Symptom
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Description
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Orphanet Frequency
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No data available
Gene & Mutation
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Gene
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Mutations
No data available
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CAS Number
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No data available
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Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References Literature
Title
PMID
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IF
No Data Found!
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