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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
Enterokinase Deficiency (ENTKD)
Alias:
Enteropeptidase Deficiency
Congenital Enteropathy Due to Enteropeptidase Deficiency
Congenital Enterokinase Deficiency
Deficiency of Enteropeptidase
Entkd
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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
肠激酶缺乏症,也称为肠肽酶缺乏症,与腹泻和心律失常性右心室心肌病有关。与肠激酶缺乏症相关的基因是TMPRSS15(跨膜丝氨酸蛋白酶15),其相关通路/超级通路包括钴胺素(Cbl,维生素B12)运输和代谢。附属组织包括小肠,相关表型为生长发育迟缓和腹泻。
Related ID:
MALACARDS:ENT006
OMIM:226200
MESH:C562649
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
--
9
59
10
ENT006
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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