Combined Oxidative Phosphorylation Deficiency 11 (COXPD11)

Alias:
Coxpd11
Combined Oxidative Phosphorylation Defect Type 11
Infantile Encephaloneuromyopathy Due to Mitochondrial Translation Defect
Encephaloneuromyopathy, Infantile, Due to Mitochondrial Translation Defect
Combined Oxidative Phosphorylation Deficiency, Type 11
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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
复合氧化磷酸化缺陷11,也称为coxpd11,与限制性皮肤病变和多小脑回有关,症状包括嗜睡和癫痫发作。与复合氧化磷酸化缺陷11有关的重要基因是RMND1(减数分裂核分裂1同源物)。相关组织包括脊髓和舌,相关表型为肝大和肌阵挛。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
7
36
9

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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