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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
Phosphoenolpyruvate Carboxykinase Deficiency
Alias:
Phosphoenolpyruvate Carboxykinase Deficiency
Pepck Deficiency
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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
磷酸烯醇丙酮酸羧激酶缺乏症,也称为磷酸烯醇丙酮酸羧激酶缺乏症,与低血糖和乳酸酸中毒有关,症状包括发绀和癫痫发作。与磷酸烯醇丙酮酸羧激酶缺乏症有关的重要基因是PCK1(磷酸烯醇丙酮酸羧激酶1),其相关通路/超级通路包括PI3K-Akt信号通路和氨基多糖代谢。附属组织包括肝脏,相关表型为PTTG1-/-和PTTG1+/+之间的负遗传相互作用。
Related ID:
MALACARDS:PHS013
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
未知
<1/1000000
2
14
--
PHS013
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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