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:

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

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
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

Title
PMID
Journal
Year
IF
No Data Found!
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