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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
非罕见病
Mitochondrial Complex I Deficiency, Nuclear Type 16 (MC1DN16)
Alias:
Mc1dn16
Mitochondrial Complex 1 Deficiency, Nuclear Type 16
Nuclear Type Mitochondrial Complex I Deficiency 16
Mi Complex I Deficiency, Nuclear Type 16
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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
线粒体复合体I缺陷,核型16,也称为mc1dn16,与湿脚气病和脚气病有关。与线粒体复合体I缺陷,核型16相关的基因是NDUFAF5(NADH:泛醌氧化还原酶复合物装配因子5),其相关通路/超级通路包括代谢和呼吸电子传递,化学耦合ATP合成,以及通过解偶联蛋白产生的热量。相关组织包括肝脏和大脑,相关表型为癫痫和痉挛。
Related ID:
MALACARDS:MTC163
OMIM:618238
MESH:D028361
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
8
36
5
MTC163
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
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Gene
Function
Score
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
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Publications
No data available
References Literature
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No Data Found!
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