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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
Mitochondrial Trifunctional Protein Deficiency (MTPD)
Alias:
Tfp Deficiency
Tfpd
Trifunctional Protein Deficiency with Myopathy and Neuropathy
Trifunctional Protein Deficiency, Type 2
Abetalipoproteinemia
Mtp Deficiency
Tpa Deficiency
Mtpd
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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
线粒体三功能蛋白缺乏症,也称为tfp缺乏症,与线粒体三功能蛋白缺乏症1和无β脂蛋白血症有关,症状包括共济失调、肌肉痛和无力。与线粒体三功能蛋白缺乏症有关的重要基因是HADHA(三功能多酶复合物亚基α-羟酰辅酶A脱氢酶),其相关通路/超级通路包括代谢和脂肪酸代谢。在该疾病的背景下提到了甘油和(3-羧基-2-(R)-羟基丙基)三甲基铵。附属组织包括肝脏和心脏,相关表型为无反射和运动耐受力低下。
Related ID:
MALACARDS:MTC027
MESH:C566945
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
1-9/100000
28
140
64
MTC027
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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