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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
Meckel Syndrome, Type 1 (MKS1)
Alias:
Meckel-Gruber Syndrome
Meckel Syndrome
Dysencephalia Splanchnocystica
Meckel Syndrome 1
Mks1
Meckel-Gruber Syndrome, Type 1
Gruber Syndrome
Mks
Mes
Meckel Syndrome Type 1
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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
梅克尔综合征1型,也称为梅克尔-格鲁伯综合征,与梅克尔综合征6型和梅克尔综合征5型有关。与梅克尔综合征1型有关的重要基因是MKS1(MKS过渡区复合物亚基1),其相关通路/超级通路包括有丝分裂中心体中Nlp的丧失和细胞器生物发生和维护。相关组织包括肾脏和脊髓,相关表型包括小头畸形和多囊肾发育不良。
Related ID:
MALACARDS:MCK013
OMIM:249000
MESH:D002925
ICD11:695796893
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
胎儿期
1-9/100000
141
998
235
MCK013
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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